[{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Research","allLocations":["San Diego, CA"]},"createdAt":1778020362831,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","id":"2e468b33-7c88-4b42-bf6f-a492a495cb73","lists":[{"text":"Responsibilities","content":"<p><span data-teams=\"true\"><strong><span style=\"text-decoration: underline;\">In Vivo Procedures</span></strong>&nbsp;</span></p>\n\n<li>Perform rodent dosing studies via intraperitoneal (IP), subcutaneous (SC), intramuscular (IM), and intratumoral (IT) routes&nbsp;</li>\n<li>Administer compounds by <strong>intravenous (IV) injection — required proficiency</strong>&nbsp;</li>\n<li>Collect biological specimens including blood via submandibular and/or cardiac puncture&nbsp;</li>\n<li>Conduct necropsies and tissue collection in accordance with approved protocols&nbsp;</li>\n<li>Support the preclinical team with daily in vivo activities and experimental procedures&nbsp;</li>\n\n<div>\n<p><strong><span style=\"text-decoration: underline;\">Animal Care &amp; Compliance</span></strong>&nbsp;</p>\n\n<li>Maintain breeding colonies, husbandry programs, and genotyping workflows&nbsp;</li>\n<li>Collect and process genotyping samples; support genotyping assay development&nbsp;</li>\n<li>Adhere to IACUC-approved protocols, policies, and all applicable regulatory requirements&nbsp;</li>\n<li>Follow established SOPs and research guidelines governing animal care and facility operations&nbsp;</li>\n\n<div>\n<p><strong><span style=\"text-decoration: underline;\">Data Collection &amp; Reporting</span></strong>&nbsp;</p>\n\n<li>Collect experimental data including body weight, blood analyses, and other project-specific measurements&nbsp;</li>\n<li>Maintain accurate and detailed records of all procedures, observations, and results&nbsp;</li>\n\n</div>\n</div>\n<div><span aria-label=\"Role Description The Animal Technician will be responsible for performing in vivo studies including compound dosing, sample collection and analysis for data generation. The position will afford the opportunity to work alongside a highly dynamic and collaborative team to develop an entirely new therapeutic modality.\" dir=\"auto\" id=\"content-1778019785620\"></span></div>"},{"text":"Requirements","content":"<div>&nbsp;</div>\n<div>\n\n<li>Bachelor's degree in a life science or related field, or equivalent hands-on research experience&nbsp;</li>\n<li>Minimum 2+ years of hands-on experience working with rodent models in a research or pharmaceutical industry&nbsp;</li>\n<li>Significant experience working with rodent models in a research or pharmaceutical setting&nbsp;</li>\n<li>Demonstrated proficiency with standard animal handling protocols and facility safety practices&nbsp;</li>\n<li>Familiarity with animal husbandry systems, welfare regulations, and institutional policies</li>\n<li><span data-teams=\"true\">Self-motivated with a strong drive to learn and contribute to organizational goals</span></li>\n<li><span data-teams=\"true\">Adaptable, with a firm commitment to scientific rigor and excellence </span></li>\n<li><span data-teams=\"true\">Highly collaborative; thrives in multidisciplinary, fast-paced research environments </span></li>\n<li><span data-teams=\"true\">Clear and effective written and verbal communication skills&nbsp;&nbsp;</span></li>\n\n</div>"}],"salaryRange":{"min":65000,"max":75000,"currency":"USD","interval":"per-year-salary"},"text":"Animal Technician, Preclinical Studies","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/2e468b33-7c88-4b42-bf6f-a492a495cb73","applyUrl":"https://jobs.lever.co/capricor/2e468b33-7c88-4b42-bf6f-a492a495cb73/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Commercial","allLocations":["San Diego, CA"]},"createdAt":1771382408438,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nAs an Associate Director / Director of Patient Advocacy at Capricor, you will guide and advance Capricor’s U.S. patient advocacy strategy across the company’s portfolio. In this role, you will cultivate trusted, compliant relationships with patient advocacy organizations, elevate the patient voice across the enterprise, and ensure patient perspectives meaningfully inform strategy from development through commercialization. The ideal candidate brings deep experience partnering with advocacy communities, strong cross functional collaboration skills, and a commitment to patient centered impact in rare and specialty disease areas.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>As an Associate Director / Director of Patient Advocacy at Capricor, you will guide and advance Capricor’s U.S. patient advocacy strategy across the company’s portfolio. In this role, you will cultivate trusted, compliant relationships with patient advocacy organizations, elevate the patient voice across the enterprise, and ensure patient perspectives meaningfully inform strategy from development through commercialization. The ideal candidate brings deep experience partnering with advocacy communities, strong cross functional collaboration skills, and a commitment to patient centered impact in rare and specialty disease areas.</div>","id":"73ecaa38-e3c4-44d7-a953-086881f7cc6c","lists":[{"text":"Responsibilities","content":"\n<li>Lead the development and execution of Capricor’s U.S. patient advocacy strategy across therapeutic areas, aligned with pipeline priorities and long term organizational goals.</li>\n<li>Identify, establish, and nurture compliant, collaborative partnerships with national and regional patient advocacy organizations.</li>\n<li>Serve as a trusted liaison between Capricor and patient communities, fostering consistent, transparent, and ethical engagement.</li>\n<li>Integrate patient insights into clinical development, Medical Affairs, Market Access, Patient Services, and Commercial activities to enhance decision making and strategy.</li>\n<li>Oversee patient listening initiatives, advisory boards, and insight gathering activities in collaboration with cross functional teams and external partners.</li>\n<li>Partner with Medical Affairs and Marketing to develop patient education resources, disease awareness initiatives, and community engagement materials.</li>\n<li>Collaborate with Policy, Access, and Patient Services teams, as well as external organizations, to understand and help address systemic barriers affecting patients and caregivers.</li>\n<li>Ensure all advocacy activities adhere to legal, regulatory, compliance, and corporate governance requirements.</li>\n<li>Track, analyze, and report on advocacy engagement, insights, and program impact to inform future planning and investment.</li>\n<li>Represent Capricor at patient focused meetings, advocacy forums, and relevant conferences to strengthen visibility and trusted engagement across communities.</li>\n"},{"text":"Requirements","content":"\n<li>Bachelor’s degree required; advanced degree in public health, health policy, communications, or a related field preferred.</li>\n<li>7–10+ years of experience in patient advocacy or patient engagement, or related external facing roles within biotech or pharma.</li>\n<li>Experience working in rare disease, specialty care, or high unmet need therapeutic areas strongly preferred.</li>\n<li>Demonstrated expertise partnering with national and regional patient advocacy organizations and community leaders.</li>\n<li>Strong understanding of compliant patient engagement practices, grants, sponsorships, and advocacy interaction requirements.</li>\n<li>Proven ability to translate patient insights into actionable inputs for clinical development, Medical Affairs, Access, and Commercial teams.</li>\n<li>Experience leading patient listening initiatives, advisory boards, or community insight gathering programs.</li>\n<li>Excellent relationship building, communication, and cross-functional collaboration skills.</li>\n<li>Ability to manage multiple external partnerships and prioritize initiatives in a fast‑paced, growth‑stage environment.</li>\n<li>Strong organizational, planning, and project‑management capabilities with a commitment to ethical, patient‑centered impact.</li>\n"}],"salaryRange":{"min":165000,"max":215000,"currency":"USD","interval":"per-year-salary"},"text":"Associate Director / Director of Patient Advocacy","country":"US","workplaceType":"remote","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>As an Associate Director / Director of Patient Advocacy at Capricor, you will guide and advance Capricor&rsquo;s U.S. patient advocacy strategy across the company&rsquo;s portfolio. In this role, you will cultivate trusted, compliant relationships with patient advocacy organizations, elevate the patient voice across the enterprise, and ensure patient perspectives meaningfully inform strategy from development through commercialization. The ideal candidate brings deep experience partnering with advocacy communities, strong cross functional collaboration skills, and a commitment to patient centered impact in rare and specialty disease areas.</div>","descriptionBodyPlain":"As an Associate Director / Director of Patient Advocacy at Capricor, you will guide and advance Capricor’s U.S. patient advocacy strategy across the company’s portfolio. In this role, you will cultivate trusted, compliant relationships with patient advocacy organizations, elevate the patient voice across the enterprise, and ensure patient perspectives meaningfully inform strategy from development through commercialization. The ideal candidate brings deep experience partnering with advocacy communities, strong cross functional collaboration skills, and a commitment to patient centered impact in rare and specialty disease areas.\n","hostedUrl":"https://jobs.lever.co/capricor/73ecaa38-e3c4-44d7-a953-086881f7cc6c","applyUrl":"https://jobs.lever.co/capricor/73ecaa38-e3c4-44d7-a953-086881f7cc6c/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"Remote","team":"Commercial","allLocations":["Remote"]},"createdAt":1766517700536,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Director / Senior Director, Channel Strategy & Patient Services will build out the distribution channel and patient support capabilities behind Capricor's U.S. launch. You will work with Commercial, Market Access, Finance, Medical, and IT, plus external trade, hub, and specialty pharmacy partners, to develop channel strategy, patient services infrastructure, and affordability programs across the portfolio.\nThis is a hands-on role owning the channel and patient services foundation and growing the function as the business scales. The right candidate has pharmaceutical distribution and patient services operations experience, works well in a growth-stage environment, and is comfortable moving between planning and execution.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><p>The Director / Senior Director, Channel Strategy &amp; Patient Services will build out the distribution channel and patient support capabilities behind Capricor's U.S. launch. You will work with Commercial, Market Access, Finance, Medical, and IT, plus external trade, hub, and specialty pharmacy partners, to develop channel strategy, patient services infrastructure, and affordability programs across the portfolio.</p>\n<p>This is a hands-on role owning the channel and patient services foundation and growing the function as the business scales. The right candidate has pharmaceutical distribution and patient services operations experience, works well in a growth-stage environment, and is comfortable moving between planning and execution.</p>","id":"c3f14202-597c-4df7-8667-31a42fadfa17","lists":[{"text":"Responsibilities","content":"<div>\n<ul type=\"disc\">\n<li>Drive Capricor’s U.S. distribution channel strategy, including 3PL selection and oversight, specialty distributor network design, trade agreements, and product flow from manufacturer to dispensing channel.</li>\n<li>Build and run Capricor’s U.S. patient services model across therapeutic areas, including referral intake, benefits investigation, prior authorization, and case management.</li>\n<li>Partner with internal teams to support the selection, onboarding, and ongoing management of 3PL, specialty distributor, hub, and specialty pharmacy partners, ensuring clear SLAs, KPIs, and governance frameworks.</li>\n<li>Map, standardize, and enhance patient journeys across programs to reduce access friction and support timely initiation of therapy.</li>\n<li>Develop and maintain SOPs and training materials for patient and provider facing interactions, ensuring alignment with regulatory, legal, and compliance expectations.</li>\n<li>Run financial assistance and affordability programs, including copay, patient assistance, and bridge/quick-start, with external vendors.</li>\n<li>Support site onboarding and certification processes for institutionally administered or infused therapies, working closely with treatment centers and operational partners.</li>\n<li>Collaborate closely with Market Access to align patient services workflows with payer requirements, reimbursement expectations, and access pathways.</li>\n<li>Partner with Commercial Operations and IT to ensure effective data capture, reporting, and system integration across vendor ecosystems.</li>\n<li>Develop dashboards, KPIs, and reporting insights to monitor program performance, patient experience, and operational effectiveness.</li>\n<li>Define KPIs and build the launch-readiness measurement framework for channel and patient services, covering pre-launch leading indicators and post-launch performance tracking.</li>\n<li>Manage relationships and budgets with channel, hub, and patient services vendors; lead RFPs and contracting in partnership with Procurement and Legal.</li>\n<li>Build a small team of patient services and channel operations staff over time, and advise Commercial leadership on how the team should grow.</li>\n<li>Run ad-hoc analyses and scenario evaluations for Commercial leadership and internal stakeholders.</li>\n<li>Establish processes, templates, and tools so channel and patient services execution stays consistent as the company grows.</li>\n\n</ul></div>"},{"text":"Requirements","content":"<div>\n<ul type=\"disc\">\n<li>Bachelor’s degree required; advanced degree or clinical background (e.g., RN, PharmD) preferred.</li>\n<li>10+ years of experience across pharmaceutical channel strategy, 3PL and specialty distribution management, patient services, hub operations, or specialty pharmacy oversight within biotech or pharma.</li>\n<li>Demonstrated success building or scaling patient support programs for rare disease or specialty therapies.</li>\n<li>Experience supporting product launches, ideally in rare diseases or complex infused therapies.</li>\n<li>Deep expertise in pharmaceutical distribution models (3PL, specialty distributor, specialty pharmacy), benefits verification, prior authorization workflows, case management, and financial assistance programs.</li>\n<li>Strong operational discipline, empathy, and vendor partnership experience.</li>\n<li>Can explain complex channel and patient services topics clearly to leadership and cross-functional teams.</li>\n<li>Proven ability to manage multiple priorities and operate effectively in a fast-paced, growth-stage environment.</li>\n<li>Has led or contributed to a commercial launch and built channel and patient services capabilities from scratch at a pre-commercial or early-commercial company.</li>\n\n</ul></div>"},{"text":"Work Environment & Physical Demands","content":"<div>\n<ul type=\"disc\">\n<li>Professional office or remote environment, with occasional travel to trade, hub, and specialty pharmacy partners, treatment centers, and internal planning meetings.</li>\n<li>Able to manage multiple priorities and cross-functional stakeholders in a launch environment.</li>\n<li>Extended periods of computer-based work, including video conferencing and collaborative software platforms.</li>\n<li>Occasional domestic travel (approximately 10 to 15%) for team meetings, vendor engagements, and industry conferences.</li>\n\n</ul></div>"}],"salaryRange":{"min":200000,"max":265000,"currency":"USD","interval":"per-year-salary"},"text":"Director / Senior Director, Channel Strategy & Patient Services","country":"US","workplaceType":"remote","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<p>The Director / Senior Director, Channel Strategy &amp; Patient Services will build out the distribution channel and patient support capabilities behind Capricor's U.S. launch. You will work with Commercial, Market Access, Finance, Medical, and IT, plus external trade, hub, and specialty pharmacy partners, to develop channel strategy, patient services infrastructure, and affordability programs across the portfolio.</p>\n<p>This is a hands-on role owning the channel and patient services foundation and growing the function as the business scales. The right candidate has pharmaceutical distribution and patient services operations experience, works well in a growth-stage environment, and is comfortable moving between planning and execution.</p>","descriptionBodyPlain":"The Director / Senior Director, Channel Strategy & Patient Services will build out the distribution channel and patient support capabilities behind Capricor's U.S. launch. You will work with Commercial, Market Access, Finance, Medical, and IT, plus external trade, hub, and specialty pharmacy partners, to develop channel strategy, patient services infrastructure, and affordability programs across the portfolio.\nThis is a hands-on role owning the channel and patient services foundation and growing the function as the business scales. The right candidate has pharmaceutical distribution and patient services operations experience, works well in a growth-stage environment, and is comfortable moving between planning and execution.\n","hostedUrl":"https://jobs.lever.co/capricor/c3f14202-597c-4df7-8667-31a42fadfa17","applyUrl":"https://jobs.lever.co/capricor/c3f14202-597c-4df7-8667-31a42fadfa17/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"Remote","team":"Commercial","allLocations":["Remote"]},"createdAt":1766517898357,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThis role will serve as the executive leader responsible for building and running the commercial infrastructure that powers Capricor's first launch, Deramiocel, our lead cell therapy for Duchenne muscular dystrophy. This role will design the end-to-end operational backbone that enables a high-performing field organization, disciplined commercial decision-making, and scalable systems across a complex rare disease and advanced-therapy landscape.\nThe ideal candidate brings deep commercial operations expertise, proven leadership launching rare disease or specialty therapies, and a hands-on builder mindset suited for a fast-growing biotech at a pivotal stage of commercialization.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><p>This role will serve as the executive leader responsible for building and running the commercial infrastructure that powers Capricor's first launch, Deramiocel, our lead cell therapy for Duchenne muscular dystrophy. This role will design the end-to-end operational backbone that enables a high-performing field organization, disciplined commercial decision-making, and scalable systems across a complex rare disease and advanced-therapy landscape.</p>\n<p>The ideal candidate brings deep commercial operations expertise, proven leadership launching rare disease or specialty therapies, and a hands-on builder mindset suited for a fast-growing biotech at a pivotal stage of commercialization.</p>","id":"f1059e4e-e2a7-450b-87fa-30dc4fcddce4","lists":[{"text":"Responsibilities","content":"<ul type=\"disc\">\n<li>Set the vision and roadmap for Commercial Operations in support of Deramiocel's launch, spanning sales operations, analytics, forecasting, incentive compensation, territory design, CRM, and commercial systems.</li>\n<li>Build and lead a high-performing Commercial Operations team and operating model tailored to a lean, launch-stage rare disease organization.</li>\n<li>Stand up the CRM ecosystem (Veeva or Salesforce), including configuration, targeting, call planning, sample management, and field reporting.</li>\n<li>Architect the commercial data environment — data warehouse and aggregator strategy (Databricks, Snowflake), dashboarding (Tableau, Power BI), and integration of claims, specialty pharmacy, HUB, patient services, and distribution data.</li>\n<li>Lead forecasting, demand planning, quota setting, territory alignment, and incentive compensation design and administration.</li>\n<li>Establish data governance, master data management, and data quality standards across the commercial organization.</li>\n<li>Partner with Market Access, Marketing, Medical Affairs, Finance, IT, Legal, and Compliance to align commercial operations with enterprise goals and ensure compliant execution.</li>\n<li>Own field force enablement — targeting, segmentation, call planning, field effectiveness analytics, and the operational elements of commercial training.</li>\n<li>Design KPI and reporting frameworks that give the Commercial Leadership Team and executive team real-time visibility into launch performance.</li>\n<li>Select, contract, and manage commercial operations vendors and service providers, including QBR ownership, SLA oversight, and budget accountability.</li>\n<li>Perform other duties as may be assigned from time to time.</li>\n</ul>"},{"text":"Requirements","content":"<div>\n<ul type=\"disc\">\n<li><strong>Education</strong>: Bachelor's degree required; MBA or other advanced degree strongly preferred.</li>\n<li><strong>Experience</strong>: 12+ years in biopharmaceutical commercial operations, including 5+ years in a leadership role and direct experience launching rare disease, advanced therapy, or specialty products.</li>\n<li><strong>Deep Expertise</strong>: Sales operations, forecasting, incentive compensation, territory alignment, CRM deployment, and commercial data strategy (claims, specialty pharmacy, HUB, distribution).</li>\n<li><strong>Executive Leadership</strong>: Demonstrated success building commercial infrastructure from the ground up, leading cross-functional initiatives, and managing strategic vendor relationships.</li>\n<li><strong>Strategic Acumen</strong>: Ability to translate commercial strategy into durable systems, processes, and analytics that drive field performance and disciplined decision-making.</li>\n\n</ul></div>"},{"text":"Work Environment & Physical Demands","content":"<div>\n<ul type=\"disc\">\n<li>Professional office or remote environment, with occasional travel for cross‑functional planning meetings and vendor engagements.</li>\n<li>Ability to manage multiple priorities in a dynamic, rapidly evolving launch environment.</li>\n<li>Extended periods of computer-based work, including video conferencing and collaborative software platforms.</li>\n<li>Domestic travel as needed (approximately 10 to 15%) for team meetings, vendor engagements, and industry conferences.</li>\n\n</ul></div>"}],"salaryRange":{"min":200000,"max":265000,"currency":"USD","interval":"per-year-salary"},"text":"Director / Senior Director, Commercial Operations & Analytics","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<p>This role will serve as the executive leader responsible for building and running the commercial infrastructure that powers Capricor's first launch, Deramiocel, our lead cell therapy for Duchenne muscular dystrophy. This role will design the end-to-end operational backbone that enables a high-performing field organization, disciplined commercial decision-making, and scalable systems across a complex rare disease and advanced-therapy landscape.</p>\n<p>The ideal candidate brings deep commercial operations expertise, proven leadership launching rare disease or specialty therapies, and a hands-on builder mindset suited for a fast-growing biotech at a pivotal stage of commercialization.</p>","descriptionBodyPlain":"This role will serve as the executive leader responsible for building and running the commercial infrastructure that powers Capricor's first launch, Deramiocel, our lead cell therapy for Duchenne muscular dystrophy. This role will design the end-to-end operational backbone that enables a high-performing field organization, disciplined commercial decision-making, and scalable systems across a complex rare disease and advanced-therapy landscape.\nThe ideal candidate brings deep commercial operations expertise, proven leadership launching rare disease or specialty therapies, and a hands-on builder mindset suited for a fast-growing biotech at a pivotal stage of commercialization.\n","hostedUrl":"https://jobs.lever.co/capricor/f1059e4e-e2a7-450b-87fa-30dc4fcddce4","applyUrl":"https://jobs.lever.co/capricor/f1059e4e-e2a7-450b-87fa-30dc4fcddce4/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Assurance","allLocations":["San Diego, CA"]},"createdAt":1777588527013,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Director, Quality Assurance & Quality Systems will lead and support quality assurance and quality systems activities for Capricor's clinical and commercial-stage biotechnology operations. The role advances the company's Quality Management System, drives inspection readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div><span data-contrast=\"auto\">The Director, Quality Assurance &amp; Quality Systems will lead and support quality assurance and quality systems activities for&nbsp;Capricor's&nbsp;clinical and commercial-stage biotechnology operations. The role advances the company's Quality Management System, drives&nbsp;inspection&nbsp;readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture.</span><span data-ccp-props=\"{&quot;335559739&quot;:240}\">&nbsp;</span></div>","id":"74178259-e3ca-4929-80ec-9dcd8bd3a73b","lists":[{"text":"Responsibilities","content":"<div>\n<p><span style=\"text-decoration: underline;\"><strong>Quality Assurance &amp; Quality Systems Leadership&nbsp;</strong></span></p>\n\n<li>Lead and manage the QA/QS team, ensuring alignment with company objectives and regulatory standards&nbsp;</li>\n<li>Develop, implement, and maintain quality management strategies and systems to ensure compliance with GMP, FDA, ICH guidelines, and other relevant regulatory bodies&nbsp;</li>\n<li>Design, establish, and continuously improve the Quality Management System (QMS), including document control, change control, training systems, and electronic quality systems (eQMS)&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Quality Systems Management&nbsp;</strong></span></p>\n\n<li>Oversee the entire quality systems infrastructure, including Standard Operating Procedures (SOPs), batch records, specifications, and validation protocols&nbsp;</li>\n<li>Manage document lifecycle management ensuring version control, approval workflows, and archival in compliance with regulatory requirements&nbsp;</li>\n<li>Establish and maintain quality metrics dashboards and Key Performance Indicators (KPIs) for system effectiveness&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Compliance &amp; Regulatory&nbsp;</strong></span></p>\n\n<li>Establish and enforce quality assurance policies and procedures across all operational departments&nbsp;</li>\n<li>Support the preparation and execution of internal audits, including regulatory inspections, to ensure compliance with regulatory requirements&nbsp;</li>\n<li>Ensure timely resolution of quality-related issues, including non-conformances, deviations, and CAPA (Corrective and Preventive Actions)&nbsp;</li>\n<li>Maintain inspection readiness and serve as primary QA point of contact for regulatory inspections&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Cross-Functional Collaboration &amp; Lifecycle Management&nbsp;</strong></span></p>\n\n<li>Collaborate with cross-functional teams (R&amp;D, manufacturing, regulatory affairs, supply chain, etc.) to ensure product quality throughout the entire lifecycle&nbsp;</li>\n<li>Partner with Regulatory Affairs to support CMC sections of regulatory submissions (IND, BLA, NDA)&nbsp;</li>\n<li>Support technology transfer activities and new product introductions from a quality systems perspective&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Continuous Improvement &amp; Risk Management&nbsp;</strong></span></p>\n\n<li>Lead continuous improvement initiatives leveraging methodologies to enhance product quality, manufacturing processes, and operational efficiency&nbsp;</li>\n<li>Provide leadership in Quality Risk Management (QRM), including identification, assessment, and mitigation of quality risks using ICH Q9 principles&nbsp;</li>\n<li>Champion a culture of quality throughout the organization&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Performance Management &amp; Reporting&nbsp;</strong></span></p>\n\n<li>Prepare and present quality performance metrics, trending analysis, and reports to senior management and board of directors&nbsp;</li>\n<li>Mentor and develop QA/QS staff, fostering a culture of accountability, compliance, and continuous professional growth&nbsp;</li>\n\n</div>"},{"text":"Requirements","content":"<div>\n<p><span style=\"text-decoration: underline;\"><strong>Education &amp; Experience&nbsp;</strong></span></p>\n\n<li>Bachelor's degree in Life Sciences, Engineering, or a related field (Master's degree preferred)&nbsp;</li>\n<li>10+ years of progressive experience in Quality Assurance and Quality Systems, with at least 5 years in a leadership role within a regulated industry (pharmaceutical, biotechnology, or medical devices)&nbsp;</li>\n<li>Direct experience in cell and gene therapy or advanced therapeutic products is highly desirable&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Technical Knowledge&nbsp;</strong></span></p>\n\n<li>Strong knowledge of regulatory requirements, including FDA, GMP, ICH guidelines, ISO 13485, and 21 CFR Parts 210, 211, 600, 820, and 1271&nbsp;</li>\n<li>Demonstrated expertise in Quality Management Systems (QMS) design, implementation, and maintenance&nbsp;</li>\n<li>Proven experience with electronic quality systems (eQMS) platforms (e.g., Veeva, MasterControl, TrackWise, or similar)&nbsp;</li>\n<li>Knowledge of Quality Risk Management methodologies (ICH Q9, FMEA, etc.)&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Leadership &amp; Management&nbsp;</strong></span></p>\n\n<li>Proven experience leading quality assurance and quality systems teams and managing cross-functional collaborations&nbsp;</li>\n<li>Demonstrated ability to drive process improvements and manage complex quality systems in dynamic environments&nbsp;</li>\n<li>Experience managing regulatory inspections and audit readiness programs&nbsp;</li>\n\n<p><span style=\"text-decoration: underline;\"><strong>Skills &amp; Competencies&nbsp;</strong></span></p>\n\n<li>Excellent problem-solving, analytical, and decision-making skills&nbsp;</li>\n<li>Strong written and verbal communication skills, with the ability to interact with senior leadership, regulatory agencies, and external stakeholders&nbsp;</li>\n<li>Experience in preparing and presenting reports and metrics to senior management and board members&nbsp;</li>\n<li>Strong leadership and interpersonal skills, with the ability to mentor and guide teams towards excellence&nbsp;</li>\n<li>Ability to work effectively in a fast-paced, entrepreneurial environment with changing priorities&nbsp;</li>\n\n</div>"},{"text":"Work Environment / Physical Demands","content":"<div>\n\n<li>Primarily office-based with required time in GMP spaces addressing quality management and audits.&nbsp;</li>\n<li>Requires prolonged periods of computer use for documentation, data analysis, and report generation related to quality processes.&nbsp;</li>\n<li>May involve lifting office materials or equipment up to 10 pounds.&nbsp;</li>\n<li>Ability to navigate office and GMP environments for audits and oversight.&nbsp;</li>\n\n</div>"}],"salaryRange":{"min":175000,"max":215000,"currency":"USD","interval":"per-year-salary"},"text":"Director, Quality Assurance & Quality Systems","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div><span xml:lang=\"EN-US\" data-contrast=\"auto\">The Director, Quality Assurance &amp; Quality Systems will lead and support quality assurance and quality systems activities for&nbsp;Capricor's&nbsp;clinical and commercial-stage biotechnology operations. The role advances the company's Quality Management System, drives&nbsp;inspection&nbsp;readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture.</span><span data-ccp-props=\"{&quot;335559739&quot;:240}\">&nbsp;</span></div>","descriptionBodyPlain":"The Director, Quality Assurance & Quality Systems will lead and support quality assurance and quality systems activities for Capricor's clinical and commercial-stage biotechnology operations. The role advances the company's Quality Management System, drives inspection readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture. \n","hostedUrl":"https://jobs.lever.co/capricor/74178259-e3ca-4929-80ec-9dcd8bd3a73b","applyUrl":"https://jobs.lever.co/capricor/74178259-e3ca-4929-80ec-9dcd8bd3a73b/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Facilities","allLocations":["San Diego, CA"]},"createdAt":1778019073637,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nWe are seeking a driven and detail-oriented Facilities Associate II / III to support and lead GMP facility operations. This individual will be responsible for independently managing equipment calibration and maintenance programs, coordinating complex vendor activities, and contributing to continuous improvement initiatives across facilities and compliance systems. The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues. This role is based at our headquarters in San Diego, CA.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>We are seeking a driven and detail-oriented Facilities Associate II / III to support and lead GMP facility operations. This individual will be responsible for independently managing equipment calibration and maintenance programs, coordinating complex vendor activities, and contributing to continuous improvement initiatives across facilities and compliance systems. The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues. This role is based at our headquarters in San Diego, CA.</div>","id":"4ed96738-2b9e-4b4a-a0c2-325bf757d2c0","lists":[{"text":"RESPONSIBILITIES","content":"\n<li>Own and manage the calibration and preventive maintenance program for GMP-critical equipment, ensuring accuracy, compliance, and timely execution.</li>\n<li>Lead the induction of new controlled assets into the inventory and maintenance tracking systems.</li>\n<li>Independently execute and improve daily, weekly, and monthly facilities operations to support manufacturing and laboratory readiness.</li>\n<li>Develop, revise, and optimize calibration and preventive maintenance schedules in alignment with operational needs and regulatory standards.</li>\n<li>Create and maintain accurate equipment documentation, including maintenance logs, procedures, and records.</li>\n<li>Schedule and coordinate maintenance and calibration work with external vendors and internal teams, ensuring minimal disruption to production and lab activities.</li>\n<li>Drive vendor qualification processes in partnership with Quality Assurance, including documentation review and audit support.</li>\n<li>Collaborate with Quality Engineering to ensure timely completion and closure of equipment work orders, deviations, and change controls.</li>\n<li>Act as a key contact for troubleshooting and resolving equipment issues, coordinating repairs and root cause analysis with vendors.</li>\n<li>Initiate and support quality records, including deviations, CAPAs, and change controls that impact GMP operations and facilities infrastructure.</li>\n<li>Identify and recommend process improvements to enhance facility efficiency, compliance, and reliability.</li>\n"},{"text":"REQUIREMENTS","content":"\n<li><span data-teams=\"true\">High school diploma or GED required. Bachelor's degree preferred, or equivalent relevant GMP experience in lieu of a degree</span></li>\n<li>3+ years of experience in a highly regulated facilities (GMP/ISO) or equipment maintenance role, ideally in biotech or pharmaceutical manufacturing.</li>\n<li>Strong understanding of GMP compliance, calibration standards, and equipment lifecycle management.</li>\n<li>Demonstrated ability to manage vendors, prioritize competing tasks, and work independently with minimal supervision.</li>\n<li>Proficiency in equipment tracking and maintenance systems; experience with CMMS or QMS software a plus.</li>\n<li>Excellent written and verbal communication skills for clear documentation and cross-functional collaboration.</li>\n<li>Exceptional organizational skills and attention to detail, with a proactive and solutions oriented mindset.</li>\n"},{"text":"Work Environment / Physical Demands:","content":"\n<li>Must be able to sit and stand for extended periods.</li>\n<li>Must be able to lift/carry reports and materials up to 40 pounds, move about the office, communicate efficiently and effectively on the telephone or in person, and complete required paperwork.<br><br></li>\n\n<div>\n<p><strong>Schedule Details:</strong></p>\n\n<li>Shift:&nbsp;<strong>Monday to Friday</strong></li>\n<li>Typical hours:&nbsp;<strong>2:00pm to 10:00 PM&nbsp;</strong>(may vary based on business needs)</li>\n<li>Flexibility is required, and occasional weekend availability for on call duties is needed.&nbsp;</li>\n\n</div>"}],"salaryRange":{"min":75000,"max":95000,"currency":"USD","interval":"per-year-salary"},"text":"Facilities Associate II / III","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>We are seeking a driven and detail-oriented Facilities Associate II / III to support and lead GMP facility operations. This individual will be responsible for independently managing equipment calibration and maintenance programs, coordinating complex vendor activities, and contributing to continuous improvement initiatives across facilities and compliance systems. The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues. This role is based at our headquarters in San Diego, CA.</div>","descriptionBodyPlain":"We are seeking a driven and detail-oriented Facilities Associate II / III to support and lead GMP facility operations. This individual will be responsible for independently managing equipment calibration and maintenance programs, coordinating complex vendor activities, and contributing to continuous improvement initiatives across facilities and compliance systems. The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues. This role is based at our headquarters in San Diego, CA.\n","hostedUrl":"https://jobs.lever.co/capricor/4ed96738-2b9e-4b4a-a0c2-325bf757d2c0","applyUrl":"https://jobs.lever.co/capricor/4ed96738-2b9e-4b4a-a0c2-325bf757d2c0/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Facilities","allLocations":["San Diego, CA"]},"createdAt":1778019525365,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","id":"be263057-5f3f-4b5b-82d2-126105df191a","lists":[{"text":"RESPONSIBILITIES","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Maintain facilities and process equipment supporting Commercial and Clinical manufacturing, Research and Development, and related services.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Manage staff to support 24/7 operations, ensuring safe,&nbsp;reliable, and cost-effective usage.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Coach, guide, and direct the facility team, monitoring and assessing performance of maintenance personnel and contractors.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Leverage&nbsp;prior&nbsp;GMP knowledge and experience to present to FDA or other regulatory agencies.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Collaborate with teams to&nbsp;identify&nbsp;and implement continuous improvement opportunities for systems and processes.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Specify and recommend equipment modifications to enhance safety, reliability, and operability.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Communicate regularly with customers, partners, and stakeholders to share key developments, opportunities, and risks.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"8\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Manage operating status and outages for systems, facilities, and utilities to maximize uptime.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"9\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Develop and implement corrective action plans for&nbsp;facility system&nbsp;repairs, replacements, and modifications.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"10\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ensure&nbsp;timely&nbsp;completion of maintenance work orders.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"11\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Track facilities expenditures and prepare the annual budget.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"12\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Foster a culture of inclusion, prioritizing&nbsp;safety&nbsp;and injury prevention.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"13\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Maintain compliance by updating maintenance and&nbsp;operations&nbsp;SOPs for improved scheduling and equipment uptime.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"48\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"14\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Perform&nbsp;additional&nbsp;assigned duties as needed.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"},{"text":"REQUIREMENTS","content":"<div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">High School Diploma/GED or local equivalent&nbsp;required;&nbsp;Bachelor’s&nbsp;degree in a relevant field preferred.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">5-8 years of relevant maintenance experience&nbsp;required.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">2-4 years of managerial experience in pharmaceuticals, biotech, food processing, high-tech, or other heavily regulated industries&nbsp;required.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">2+ years of experience managing facilities under GMP regulatory compliance&nbsp;required.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Comprehensive knowledge of maintenance practices for equipment such as boilers, chillers, air handlers, HVAC systems, cooling towers, pure steam generators, Water for Injection systems, autoclaves, heat exchangers, security systems, electrical distribution, fire protection, clean-in-place systems, classified air systems, RODI systems, emergency generators, and fume exhaust systems.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Familiarity with pharmaceutical manufacturing equipment, including liquid filling machines,&nbsp;stoppering&nbsp;machines, capping machines, vial washers, and dehydrogenation ovens.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to manage multiple responsibilities with strong self-motivation.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"8\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Capability to work independently and collaboratively in a team-oriented environment.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"9\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Trained in cGMP operations for pharmaceutical, biotechnology, or medical device manufacturing.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"10\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Knowledge of aseptic gowning and cleaning techniques.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"11\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Proficiency&nbsp;in managing after-hours&nbsp;responses and extended shifts to support planned or unplanned events.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"12\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Strong analytical, problem-solving, and communication skills.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"49\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"13\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Leadership skills to guide and coach teams effectively.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"},{"text":"Work Environment / Physical Demands:","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Primarily facility-based, involving oversight of manufacturing and R&amp;D systems, with tasks including maintenance, inspections, and documentation.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Requires accessing small spaces to assess mechanical issues and standing or walking for extended periods.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Involves prolonged periods of computer use for tracking expenditures, preparing budgets, and updating SOPs.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">May require&nbsp;lifting up&nbsp;to 50 pounds.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">May involve after-hours&nbsp;responses and extended shifts to support facility operations.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"50\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Occasional travel may be&nbsp;required&nbsp;for regulatory presentations or vendor interactions.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"}],"salaryRange":{"min":120000,"max":140000,"currency":"USD","interval":"per-year-salary"},"text":"Facilities Manager","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/be263057-5f3f-4b5b-82d2-126105df191a","applyUrl":"https://jobs.lever.co/capricor/be263057-5f3f-4b5b-82d2-126105df191a/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n \nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n \nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n \n \n \nNotice to Recruiting Agencies\nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><strong>Why Capricor?</strong></div>\n<div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div>\n<div>&nbsp;</div>\n<div><strong>Come Work With Us!</strong></div>\n<div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div>\n<div>&nbsp;</div>\n<div><em>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</em></div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>Notice to Recruiting Agencies</div>\n<div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"Remote","team":"Quality Compliance","allLocations":["Remote"]},"createdAt":1773248609824,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n \nThe License Associate III will lead and coordinate the preparation, submission, and maintenance of initial facility and establishment license applications for drug manufacturing and tissue operations in the United States, European Union, and Japan.\nThis role is pivotal in ensuring the company’s manufacturing sites and partner facilities are fully licensed and compliant with GMP (Good Manufacturing Practice), GTP (Good Tissue Practice), and regional ATMP regulatory frameworks. The successful candidate will collaborate closely with key stakeholders to support global launch readiness and regulatory compliance for advanced therapy products.\n","description":"<div><span style=\"font-size: 16px;\">Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;Deramiocel&nbsp;(</span><em style=\"font-size: 16px;\">CAP-1002</em><span style=\"font-size: 16px;\">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</span></div>\n<div>&nbsp;</div>\n<div><span style=\"font-size: 16px;\">The License Associate III will lead and coordinate the preparation, submission, and maintenance of initial facility and establishment license applications for drug manufacturing and tissue operations in the United States, European Union, and Japan.</span></div>\n<div><span style=\"font-size: 16px;\">This role is pivotal in ensuring the company’s manufacturing sites and partner facilities are fully licensed and compliant with GMP (Good Manufacturing Practice), GTP (Good Tissue Practice), and regional ATMP regulatory frameworks. The successful candidate will collaborate closely with key stakeholders to support global launch readiness and regulatory compliance for advanced therapy products.</span></div>","id":"0e395722-8f55-4066-80bf-4113d7a1545b","lists":[{"text":"Key Responsibilities:","content":"\n<li>Prepare and compile initial license application dossiers including:</li>\n\n<div>FDA Establishment Registration and Tissue Establishment Registration (21 CFR Part 1271)</div>\n<div>EU Manufacturing Authorisation and Tissue Establishment Licence (2004/23/EC, 1394/2007/EC)</div>\n<div>PMDA/MHLW Manufacturing and Processing Licence applications (Japanese GMP/GCTP framework)</div>\n\n<li>Track submission progress and maintain clear communication with health authorities and notified bodies.</li>\n\n\n<li>Ensure ongoing compliance with applicable GMP, GTP, and GCTP standards.</li>\n<li>Support audit and inspection readiness activities related to establishment licensing.</li>\n<li>Monitor changes in cell therapy, ATMP, and tissue regulations; provide impact assessments and guidance to management.</li>\n<li>Maintain a global register of active licenses, renewals, and regulatory commitments.</li>\n\n\n<li>Serve as the point of contact for FDA, EMA, MHRA, PMDA, and local competent authorities on establishment and tissue-related matters.</li>\n<li>Coordinate with regional consultants and partners to manage local, national and international licensing submissions and renewals.</li>\n<li>Support due diligence activities for partnerships or facility expansions.</li>\n"},{"text":"Requirements ","content":"\n<li>Bachelor’s or advanced degree in Life Sciences, Pharmacy, Biotechnology, or Regulatory Affairs.</li>\n<li>Minimum 5 years of experience in Regulatory Affairs within cell therapy, gene therapy, tissue banking, or biologics manufacturing.</li>\n<li>Demonstrated success preparing or managing initial site or establishment license applications across multiple regions.</li>\n<li>Solid understanding of ATMP/biologics manufacturing regulatory frameworks in the USA (FDA), EU (EMA), and Japan (PMDA/MHLW).</li>\n<li>Working knowledge of:</li>\n\n<div>21 CFR Parts 210, 211, 1271 (GMP/GTP – USA)</div>\n<div>EU Directives 2001/83/EC, 2004/23/EC, Regulation (EC) 1394/2007 (ATMP – EU)</div>\n<div>Japanese GCTP and PMDA Manufacturing Licence Regulations (Japan)</div>"}],"salaryRange":{"min":90000,"max":99000,"currency":"USD","interval":"per-year-salary"},"text":"License Associate III","country":"US","workplaceType":"hybrid","opening":"","openingPlain":"","descriptionBody":"<div><span style=\"font-size: 16px;\">Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;Deramiocel&nbsp;(</span><em style=\"font-size: 16px;\">CAP-1002</em><span style=\"font-size: 16px;\">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX&trade; exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</span></div>\n<div>&nbsp;</div>\n<div><span style=\"font-size: 16px;\">The License Associate III will lead and coordinate the preparation, submission, and maintenance of initial facility and establishment license applications for drug manufacturing and tissue operations in the United States, European Union, and Japan.</span></div>\n<div><span style=\"font-size: 16px;\">This role is pivotal in ensuring the company&rsquo;s manufacturing sites and partner facilities are fully licensed and compliant with GMP (Good Manufacturing Practice), GTP (Good Tissue Practice), and regional ATMP regulatory frameworks. The successful candidate will collaborate closely with key stakeholders to support global launch readiness and regulatory compliance for advanced therapy products.</span></div>","descriptionBodyPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n \nThe License Associate III will lead and coordinate the preparation, submission, and maintenance of initial facility and establishment license applications for drug manufacturing and tissue operations in the United States, European Union, and Japan.\nThis role is pivotal in ensuring the company’s manufacturing sites and partner facilities are fully licensed and compliant with GMP (Good Manufacturing Practice), GTP (Good Tissue Practice), and regional ATMP regulatory frameworks. The successful candidate will collaborate closely with key stakeholders to support global launch readiness and regulatory compliance for advanced therapy products.\n","hostedUrl":"https://jobs.lever.co/capricor/0e395722-8f55-4066-80bf-4113d7a1545b","applyUrl":"https://jobs.lever.co/capricor/0e395722-8f55-4066-80bf-4113d7a1545b/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Supply Chain","allLocations":["San Diego, CA"]},"createdAt":1770767955287,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Sr. Manager / Manager of Commercial Logistics is responsible for leading end-to-end commercial distribution operations for Capricor’s drug products. This role oversees GxP-compliant logistics, cold-chain distribution, third-party logistics (3PL) management, serialization, and DSCSA compliance. The position ensures products are stored, handled, serialized, and delivered to customers, partners, depots, and distributors in full alignment with regulatory and quality requirements.\n\nThis leader will partner cross-functionally with Supply Chain, Quality, Commercial, Manufacturing, CMC, and external logistics and serialization partners to build and manage robust commercial distribution and compliance processes that support product launch and commercial growth.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>The Sr. Manager / Manager of Commercial Logistics is responsible for leading end-to-end commercial distribution operations for Capricor’s drug products. This role oversees GxP-compliant logistics, cold-chain distribution, third-party logistics (3PL) management, serialization, and DSCSA compliance. The position ensures products are stored, handled, serialized, and delivered to customers, partners, depots, and distributors in full alignment with regulatory and quality requirements.</div><div><br></div><div>This leader will partner cross-functionally with Supply Chain, Quality, Commercial, Manufacturing, CMC, and external logistics and serialization partners to build and manage robust commercial distribution and compliance processes that support product launch and commercial growth.</div>","id":"d27ce56f-4be7-403f-be88-b4f91f41f1a6","lists":[{"text":"Responsibilities","content":"<li><i>The responsibilities of this job include, but are not limited to:</i></li><div><br></div><div><b>Commercial Distribution &amp; Logistics Management</b></div><li>Lead day-to-day oversight of commercial distribution activities for drug product shipments (domestic and international).</li><li>Manage commercial cold-chain distribution, ensuring product integrity, temperature-controlled packaging, lane qualification, and monitoring.</li><li>Develop and maintain logistics processes for order fulfillment, shipment tracking, delivery confirmation, and exception handling.</li><li>Ensure all activities comply with GDP/GxP, FDA/ICH regulations, and internal SOPs.</li><li>Oversee the receiving, collection, and handoff of finished goods (FG) from manufacturing, including flexible hour coverage as required to support real-time production and release schedules.</li><div><br></div><div><b>Assembly Components &amp; Pack-Out Management</b></div><li>Manage assembly components required for commercial pack-out, including storage, issuance, staging, and reconciliation of all packaging materials.</li><li>Coordinate with Quality, Packaging Vendors, Manufacturing, and 3PLs to ensure pack-out kits are complete, compliant, and available when needed.</li><div><br></div><div><b>3PL / External Partner Oversight</b></div><li>Serve as the primary operational lead for 3PLs, couriers, packaging providers, and commercial distribution partners.</li><li>Monitor 3PL performance via metrics, QBRs, and contract commitments.</li><li>Manage distribution agreements, service levels, capacity planning, and cost control.</li><li>Lead issue resolution for shipment deviations, temperature excursions, and supply disruptions.</li><div><br></div><div><b>Serialization &amp; DSCSA Compliance</b></div><li>Own and govern end-to-end serialization and DSCSA business processes across packaging, distribution, and trading partners, ensuring compliance with U.S. and international regulatory requirements and internal quality standards.</li><li>Act as the primary business lead for serialization systems and data flows (e.g., product identifiers, aggregation, EPCIS).</li><li>Partner closely with IT, Quality Engineering, Supply Chain, and external serialization vendors to drive system maintenance, issue resolution, and continuous improvement.</li><li>Monitor regulatory changes, compliance metrics, and operational performance related to serialization and DSCSA obligations.</li><li>Lead deviations, investigations, and remediation activities for serialization, EPCIS data, system failures, and DSCSA compliance gaps.</li><li>Collaborate with IT and Supply Chain to ensure accurate ERP configuration, data integrity, and process alignment for order management, inventory control, distribution workflows, and serialization integration.</li><div><br></div><div><b>Launch Readiness &amp; Commercial Expansion</b></div><li>Support global launch planning, including route-to-market strategy, depot set-up, trade/distribution model design, and packaging/labeling logistics.</li><li>Build scalable processes to support product growth, new indications, and geographic expansion.</li><li>Collaborate with Commercial and Finance to develop demand forecasts and distribution plans.</li><div><br></div><div><b>Compliance, Documentation &amp; Quality Support</b></div><li>Maintain GDP-compliant documentation, including shipping records, temperature logs, investigations, and change controls.</li><li>Partner with Quality to support audits, lot release logistics, and inspection readiness.</li><li>Author and maintain shipping, distribution, and serialization SOPs and training materials.</li><li>Ensure that all onboarding, receipt, and control of packaging components, pack-out materials, and finished goods follow company inventory policies and are fully aligned with ERP/serialization tracking requirements.</li><div><br></div><div><b>Operational Excellence &amp; Continuous Improvement</b></div><li>Analyze logistics and serialization performance metrics to identify improvement opportunities.</li><li>Implement best practices across packaging, freight optimization, cold-chain technologies, and distribution risk mitigation.</li><li>Support business continuity planning and supply chain resilience initiatives.</li><div><br></div><div><b>Team Management</b></div><li>Directly supervises the Commercial Logistics Supervisor and Shipping Associates responsible for daily shipping, receiving, and finished goods handling.</li><li>Provides coaching, development, and performance management to logistics team members.</li><li>Oversees workload planning, training, and staffing to support commercial operations.</li><li>This team will expand as commercial volumes grow, and the Sr. Manager/Manager will lead future hiring and organization development.</li>"},{"text":"Requirements","content":"<li>Bachelor’s degree in Supply Chain, Business, Life Sciences, Engineering, or related field.</li><li><b>Manager level:</b> 6+ years of logistics, distribution, or supply chain experience in pharmaceuticals or biotech.</li><li><b>Sr. Manager level:</b> 8+ years of logistics, distribution, or supply chain experience in pharmaceuticals or biotech.</li><li>Strong understanding of GDP/GxP requirements, biologics handling, and commercial distribution.</li><li>Hands-on experience with serialization and DSCSA compliance (EPCIS, aggregation, product identifier management).</li><li>Experience working with ERP systems (e.g., NetSuite, SAP, Oracle) for order management, inventory, and distribution processes.</li><li>Experience managing 3PL vendors and commercial distribution centers.</li><li>Strong communication, analytical, and cross-functional collaboration skills.</li>"},{"text":"Preferred Qualifications","content":"<li>Experience supporting commercial product launches in pharma/biotech.</li><li>Knowledge of cell therapy, gene therapy, or advanced biologics distribution.</li><li>Experience with ERP/WMS systems (e.g., NetSuite, SAP, Oracle), serialization platforms, and EPCIS data tools.</li><li>ASCM certified / CLTD (Certified in Logistics, Transportation and Distribution) or related field preferred; equivalent experience considered.</li><li>Strong knowledge of domestic and international shipping regulations (DOT, IATA).</li><li>Project management certification or experience leading cross-functional initiatives.</li><li>Understanding of import/export regulations, customs processes, and global cold-chain requirements.</li>"},{"text":"Competency Definitions","content":"<li>Strong problem-solving and decision-making ability.</li><li>Vendor management and negotiation skills.</li><li>Ability to work in a fast-paced, rapidly scaling environment.</li><li>Exceptional attention to detail and documentation discipline.</li><li>Ability to influence without authority across cross-functional teams.</li>"},{"text":"Working Conditions","content":"<li>Office and warehouse environment.</li><li>Occasional travel to 3PLs, packaging vendors, manufacturing sites, or logistics providers.</li>"}],"salaryRange":{"min":115000,"max":154000,"currency":"USD","interval":"per-year-salary"},"text":"Manager / Senior Manager, Commercial Logistics","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>The Sr. Manager / Manager of Commercial Logistics is responsible for leading end-to-end commercial distribution operations for Capricor’s drug products. This role oversees GxP-compliant logistics, cold-chain distribution, third-party logistics (3PL) management, serialization, and DSCSA compliance. The position ensures products are stored, handled, serialized, and delivered to customers, partners, depots, and distributors in full alignment with regulatory and quality requirements.</div><div><br></div><div>This leader will partner cross-functionally with Supply Chain, Quality, Commercial, Manufacturing, CMC, and external logistics and serialization partners to build and manage robust commercial distribution and compliance processes that support product launch and commercial growth.</div>","descriptionBodyPlain":"The Sr. Manager / Manager of Commercial Logistics is responsible for leading end-to-end commercial distribution operations for Capricor’s drug products. This role oversees GxP-compliant logistics, cold-chain distribution, third-party logistics (3PL) management, serialization, and DSCSA compliance. The position ensures products are stored, handled, serialized, and delivered to customers, partners, depots, and distributors in full alignment with regulatory and quality requirements.\n\nThis leader will partner cross-functionally with Supply Chain, Quality, Commercial, Manufacturing, CMC, and external logistics and serialization partners to build and manage robust commercial distribution and compliance processes that support product launch and commercial growth.\n","hostedUrl":"https://jobs.lever.co/capricor/d27ce56f-4be7-403f-be88-b4f91f41f1a6","applyUrl":"https://jobs.lever.co/capricor/d27ce56f-4be7-403f-be88-b4f91f41f1a6/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-time (non-exempt)","department":"Capricor Therapeutics","location":"San Diego - SD1","team":"Manufacturing","allLocations":["San Diego - SD1"]},"createdAt":1778690931103,"description":"","descriptionPlain":"","id":"d1d33e21-fc8f-4328-9e62-31a169b5da7b","lists":[{"text":"Responsibilities","content":"<div>\n\n<li>Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing.</li>\n<li>Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols.</li>\n<li>Mentor fellow team members on cGMP documentation protocols to ensure the highest standards.</li>\n<li>Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations.</li>\n<li>Author, revise, and maintain SOPs through Capricor’s document change system.</li>\n<li>Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations.</li>\n<li>Prepare technical summaries, protocols, and reports to ensure full documentation of production activities.</li>\n<li>Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance.</li>\n<li>Take on special projects in manufacturing and development as required.</li>\n\n</div>"},{"text":"Requirements","content":"<div>\n\n<li>Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field.</li>\n<li>1-3 years of experience in a cGMP/cGTP manufacturing environment.</li>\n<li>Solid laboratory experience in mammalian tissue culture, along with expertise in aseptic techniques.</li>\n<li>Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries.</li>\n<li>Strong organizational skills and acute attention to detail within a fast-paced, dynamic setting.</li>\n<li>Basic molecular biology and flow cytometry skills are a plus.</li>\n<li>Adaptability to work schedules that may include weekends or holidays as needed.</li>\n\n</div>"}],"salaryRange":{"min":25,"max":30,"currency":"USD","interval":"per-hour-wage"},"text":"Manufacturing Associate I","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/d1d33e21-fc8f-4328-9e62-31a169b5da7b","applyUrl":"https://jobs.lever.co/capricor/d1d33e21-fc8f-4328-9e62-31a169b5da7b/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n \nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n \nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n \n \n \nNotice to Recruiting Agencies\nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n \n \n","additional":"<div>\n<div>\n<div>\n<div>\n<div data-qa=\"closing-description\">\n<div><strong>Why Capricor?</strong></div>\n<div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div>\n<div>&nbsp;</div>\n<div><strong>Come Work With Us!</strong></div>\n<div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div>\n<div>&nbsp;</div>\n<div><em>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</em></div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>Notice to Recruiting Agencies</div>\n<div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>\n</div>\n<div data-qa=\"btn-apply-bottom\">&nbsp;</div>\n</div>\n</div>\n</div>\n<div>\n<div>&nbsp;</div>\n</div>\n</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Manufacturing","allLocations":["San Diego, CA"]},"createdAt":1774888187012,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n \nAs a Manufacturing Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials. You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>\n<div>&nbsp;</div>\n<div>As a Manufacturing Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials. You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence.&nbsp;</div>","id":"31aa4138-822e-41a7-aeaa-4fedd04c0fa4","lists":[{"text":"Responsibilities","content":"<div>\n<p>· Supervise the manufacturing team, including Technicians, Associates (I-II, III, III-Lead), to ensure seamless execution of production tasks such as cell culture, media preparation, formulation, centrifugation, and freezing.</p>\n<p>· Ensure all manufacturing activities comply with cGMP standards, overseeing proper documentation, inventory management, and cleanroom operations.</p>\n<p>· Review and approve cGMP documentation, including batch records, logs, forms, and protocols, ensuring accuracy and adherence to Good Documentation Practices (GDP).</p>\n<p>· Monitor production processes, analyze data, and report on performance metrics to identify areas for improvement and ensure quality goals are met.</p>\n<p>· Coordinate with the Associate Director of Manufacturing to develop production schedules, allocate resources, and address operational challenges.</p>\n<p>· Lead training and mentoring of manufacturing staff, ensuring team competency in aseptic techniques, cGMP standards, and manufacturing procedures.</p>\n<p>· Oversee the initiation, investigation, and closure of deviations, CAPAs, and process improvements, ensuring timely resolution and documentation.</p>\n<p>· Author, review, and update standard operating procedures (SOPs) and other manufacturing documentation using the document change system.</p>\n<p>· Manage inventory, material transfers, and cleanroom setup/shutdown activities to support continuous manufacturing operations.</p>\n<p>· Facilitate cross-functional collaboration with Quality Control, Materials Management, and other departments to ensure production alignment with company objectives.</p>\n<p>· Lead special manufacturing and development projects as assigned by the Associate Director of Manufacturing.</p>\n<p>· Perform other duties as assigned to support manufacturing operations and company goals.</p>\n</div>"},{"text":"Requirements","content":"<div>\n<p>· Bachelor’s degree in Biological Sciences, Biomedical Engineering, or related field; advanced degree preferred.</p>\n<p>· 6+ years of experience in a cGMP manufacturing environment, with at least 2-3 years in a supervisory or leadership role.</p>\n<p>· In-depth knowledge of cell culture, aseptic techniques, cGMP standards, and regulatory compliance in a biotech/pharma setting.</p>\n<p>· Proven expertise in Good Documentation Practices (GDP) and managing manufacturing documentation.</p>\n<p>· Experience leading deviation investigations, CAPAs, and process improvement initiatives.</p>\n<p>· Strong leadership and mentoring skills, with the ability to guide and develop a diverse manufacturing team.</p>\n<p>· Excellent organizational and problem-solving skills, with the ability to manage multiple priorities in a fast-paced environment.</p>\n<p>· Effective communication skills for cross-functional collaboration, training, and reporting to senior management.</p>\n<p>· Proficiency in data analysis, technical report writing, and presenting production metrics.</p>\n<p>· Ability to gown and work in classified cleanroom areas, ensuring compliance with ISO 7 standards.</p>\n</div>"},{"text":"Work Environment / Physical Demands","content":"<div>\n<p>· Primarily cleanroom-based with required time in GMP spaces overseeing manufacturing operations and team activities.</p>\n<p>· Requires prolonged periods of standing, computer use for documentation and reporting, and full gowning in ISO 7 cleanroom.</p>\n<p>· May involve lifting materials or equipment up to 20 pounds.</p>\n<p>· Ability to navigate cleanroom and GMP environments for production oversight and staff training.</p>\n</div>"}],"salaryRange":{"min":100000,"max":118000,"currency":"USD","interval":"per-year-salary"},"text":"Manufacturing Supervisor","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX&trade; exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>\n<div>&nbsp;</div>\n<div>As a Manufacturing Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials. You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence.&nbsp;</div>","descriptionBodyPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n \nAs a Manufacturing Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials. You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence. \n","hostedUrl":"https://jobs.lever.co/capricor/31aa4138-822e-41a7-aeaa-4fedd04c0fa4","applyUrl":"https://jobs.lever.co/capricor/31aa4138-822e-41a7-aeaa-4fedd04c0fa4/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-time (non-exempt)","department":"Capricor Therapeutics","location":"San Diego - SD1","team":"Manufacturing","allLocations":["San Diego - SD1"]},"createdAt":1778690708608,"description":"","descriptionPlain":"","id":"300b5c57-c619-466d-a592-935fac827687","lists":[{"text":"Responsibilities","content":"<div>\n\n<li>Maintaining cleanroom inventory, performing material transfers and cleanroom-required activities to support cGMP operations (i.e restocking Kanban, scrubs, and gowning)&nbsp;</li>\n<li>Ensuring clear communication and working closely with manufacturing and materials management to confirm proper materials are stocked accordingly;&nbsp;</li>\n<li>Performing cleanroom setup and shutdown (Biohazard waste decontamination, packaging and autoclaving of required materials/supplies, etc)&nbsp;</li>\n<li>Performing special manufacturing projects&nbsp;</li>\n<li>Completing required documentation with proper cGMP recording of entries and comments on batch records, forms and protocols independently;&nbsp;</li>\n<li>Operation, Maintenance, and Cleaning of GMP equipment, including: Centrifuges, Microscopes, Incubators, BSCs, Refrigerators, Freezers, etc&nbsp;</li>\n<li>Initiate minor revisions to existing documents, to troubleshoot simple existing procedures, and to contribute to continuous improvement initiatives. &nbsp;</li>\n<li>Performing such other duties as may be assigned from time to time.&nbsp;</li>\n\n</div>"},{"text":"Requirements","content":"<div>\n\n<li>High school diploma or GED required&nbsp;</li>\n<li>Lift, push, pull and carry up to 40 lbs.&nbsp;</li>\n<li>Excellent knowledge of aseptic technique and aseptic practices&nbsp;</li>\n<li>Exceptional communication and interpersonal skills&nbsp;</li>\n<li>Excellent organizational skills and attention to detail&nbsp;</li>\n<li>Excellent interpersonal skills, team player&nbsp;</li>\n<li>Ability to work in a dynamic environment&nbsp;</li>\n<li>Adaptable/flexible with work schedule with an ability to multi-task and prioritize work &nbsp;</li>\n<li>From time-to-time extended hours may be required with or without notice, dependent on the work needed&nbsp;</li>\n<li>Occasional weekend work may be required&nbsp;</li>\n\n</div>"},{"text":"Preferred ","content":"<div>\n\n<li>Bachelor’s degree in Biology, Biological Sciences or related field preferred&nbsp;</li>\n<li>1+ years of experience in GMP/cGMP manufacturing environment in academic/industry setting&nbsp;</li>\n<li>Excellent knowledge of Good Documentation Practices&nbsp;</li>\n\n</div>"}],"salaryRange":{"min":23,"max":25,"currency":"USD","interval":"per-hour-wage"},"text":"Manufacturing Technician","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/300b5c57-c619-466d-a592-935fac827687","applyUrl":"https://jobs.lever.co/capricor/300b5c57-c619-466d-a592-935fac827687/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"Remote","team":"Medical Affairs","allLocations":["Remote"]},"createdAt":1780367592199,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Medical Science Liaison (MSL) Director is a field-based scientific leader responsible for delivering Capricor's scientific engagement strategy across an assigned territory of national and regional KOLs treating Duchenne muscular dystrophy (DMD) and DMD cardiomyopathy. The role focuses on scientific exchange with thought leaders, treatment centers, and academic institutions in neuromuscular disease, cardiology, and pediatric specialty care; identification of clinical and research opportunities; and translation of field insights into Capricor's medical strategy for Deramiocel. This individual partners closely with the Medical Director, VP Medical Affairs, HEOR / RWE, Pharmacovigilance, Clinical Development, and the broader U.S. MSL team.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>The Medical Science Liaison (MSL) Director is a field-based scientific leader responsible for delivering Capricor's scientific engagement strategy across an assigned territory of national and regional KOLs treating Duchenne muscular dystrophy (DMD) and DMD cardiomyopathy. The role focuses on scientific exchange with thought leaders, treatment centers, and academic institutions in neuromuscular disease, cardiology, and pediatric specialty care; identification of clinical and research opportunities; and translation of field insights into Capricor's medical strategy for Deramiocel. This individual partners closely with the Medical Director, VP Medical Affairs, HEOR / RWE, Pharmacovigilance, Clinical Development, and the broader U.S. MSL team.</div>","id":"6d48a585-ca4b-439d-b471-bfe9a1e4d8da","lists":[{"text":"Responsibilities","content":"<div>• Develop and execute the territory KOL/HCP engagement plan, including identification, mapping, and prioritization of thought leaders, prescribers and treatment centers.<br>• Deliver scientific presentations and engage in scientific exchange with KOLs and HCPs on Deramiocel clinical data, the DMD cardiomyopathy landscape, and emerging evidence.<br>• Support advisory boards, scientific symposia, and KOL-led research initiatives.<br>• Identify and support investigator-initiated studies (IIS) and real-world evidence opportunities in coordination with HEOR / RWE and Medical Director.<br>• Provide scientific support for medical congresses, including DMD, neuromuscular, cardiology, and rare-disease forums.<br>• Collect and synthesize field insights on clinical practice, treatment decision-making, and emerging evidence; translate insights into recommendations for medical strategy.<br>• Provide scientific training and support to internal stakeholders (Sales, Market Access, Patient Services) in compliance with channel and engagement rules.<br>• Maintain comprehensive scientific fluency on Deramiocel clinical data, DMD natural history, and the broader treatment landscape.<br>• Ensure timely reporting of adverse events and product complaints in line with company and regulatory processes.<br>• Document field activities, KOL/HCP engagement, and insights in Capricor's medical CRM in compliance with standards.<br>• Ensure all activities follow FDA, OIG, PhRMA Code, ACCME, and Capricor compliance standards.<br>• Perform other duties as may be assigned from time to time.</div>"},{"text":"Required Qualifications","content":"<div>• Advanced clinical degree required (MD, PharmD, PhD, DO, or equivalent).<br>• 5 to 10 years of MSL experience in biotech / pharma; experience in rare disease, cell / gene therapy, pediatrics, neuromuscular disease, or cardiology preferred.<br>• Established scientific credibility and ability to engage KOLs in peer-to-peer scientific exchange.<br>• Strong working knowledge of FDA, OIG, PhRMA Code, ACCME, and MLR review processes.<br>• Excellent written and verbal scientific communication skills, including ability to deliver complex data to clinical audiences.<br>• Self-directed execution and the ability to operate independently in a field-based environment.</div>"},{"text":"Preferred Qualifications","content":"<div>• Existing relationships across the DMD treatment center network, neuromuscular community, or pediatric cardiology community.<br>• Prior launch experience in rare disease, cell / gene therapy, pediatrics, rare cardiology or neuromuscular disease.<br>• Experience operating in a pre-commercial or early-commercial company.</div>"},{"text":"Competency Definitions","content":"<div>• Strong problem-solving and decision-making ability.<br>• Vendor management and negotiation skills.<br>• Ability to work in a fast-paced, rapidly scaling environment.<br>• Exceptional attention to detail and documentation discipline.<br>• Ability to influence without authority across cross-functional teams.</div>"},{"text":"Working Conditions","content":"<div>• Field-based (remote) position based in or near the assigned territory; territory geography determined at hire.<br>• Domestic travel approximately 60 to 75% for KOL engagement, advisory boards, congresses, and internal planning.<br>• Periodic presence at Capricor's San Diego HQ as required by business need.</div>"}],"salaryRange":{"min":200000,"max":250000,"currency":"USD","interval":"per-year-salary"},"text":"Medical Science Liaison (MSL) Director","country":"US","workplaceType":"remote","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>The Medical Science Liaison (MSL) Director is a field-based scientific leader responsible for delivering Capricor's scientific engagement strategy across an assigned territory of national and regional KOLs treating Duchenne muscular dystrophy (DMD) and DMD cardiomyopathy. The role focuses on scientific exchange with thought leaders, treatment centers, and academic institutions in neuromuscular disease, cardiology, and pediatric specialty care; identification of clinical and research opportunities; and translation of field insights into Capricor's medical strategy for Deramiocel. This individual partners closely with the Medical Director, VP Medical Affairs, HEOR / RWE, Pharmacovigilance, Clinical Development, and the broader U.S. MSL team.</div>","descriptionBodyPlain":"The Medical Science Liaison (MSL) Director is a field-based scientific leader responsible for delivering Capricor's scientific engagement strategy across an assigned territory of national and regional KOLs treating Duchenne muscular dystrophy (DMD) and DMD cardiomyopathy. The role focuses on scientific exchange with thought leaders, treatment centers, and academic institutions in neuromuscular disease, cardiology, and pediatric specialty care; identification of clinical and research opportunities; and translation of field insights into Capricor's medical strategy for Deramiocel. This individual partners closely with the Medical Director, VP Medical Affairs, HEOR / RWE, Pharmacovigilance, Clinical Development, and the broader U.S. MSL team.\n","hostedUrl":"https://jobs.lever.co/capricor/6d48a585-ca4b-439d-b471-bfe9a1e4d8da","applyUrl":"https://jobs.lever.co/capricor/6d48a585-ca4b-439d-b471-bfe9a1e4d8da/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"MSAT","allLocations":["San Diego, CA"]},"createdAt":1779485661002,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or biologics manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities. \n \nIn this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div><span style=\"font-size: 10.5pt;\">The MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or&nbsp;biologics&nbsp;manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities.&nbsp;</span></div>\n<div>&nbsp;</div>\n<div><span style=\"font-size: 10.5pt;\">In this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations.&nbsp;</span></div>","id":"1b1ec559-3f4b-46c9-89a4-feaa9561e828","lists":[{"text":"Responsibilities","content":"\n<li>Providing&nbsp;support&nbsp;to MSAT Team&nbsp;and working cross-functionally&nbsp;to&nbsp;ensure clear communication&nbsp;across various departments.&nbsp;&nbsp;</li>\n<li>Management of deviations and other quality records, performing&nbsp;root cause&nbsp;investigations&nbsp;(6M, 5-Why’s,&nbsp;etc)&nbsp;to&nbsp;determine&nbsp;causal factors&nbsp;and&nbsp;evaluate&nbsp;product impact.&nbsp;</li>\n<li>Training&nbsp;on&nbsp;the cell&nbsp;therapy and/or&nbsp;exosome platforms&nbsp;quickly to&nbsp;assist&nbsp;in&nbsp;product impact&nbsp;assessments, and&nbsp;compiling&nbsp;scientific data relating&nbsp;to&nbsp;the&nbsp;manufacturing processes.&nbsp;</li>\n<li>Assisting&nbsp;with&nbsp;tech transfers into&nbsp;cGMP Manufacturing,&nbsp;ensuring&nbsp;the transfer is&nbsp;controlled and executed within GMP regulatory guidelines.&nbsp;</li>\n<li>Supporting Manufacturing group and troubleshooting production activities to ensure safe, quality, and&nbsp;timely&nbsp;manufacture of biopharmaceutical&nbsp;product&nbsp;for pre-clinical,&nbsp;clinical&nbsp;and commercial use.&nbsp;</li>\n<li>Assisting&nbsp;on revising&nbsp;(as needed) and reviewing process-related manufacturing documentation (batch records,&nbsp;SOPs, bills of material, process flow diagrams) to&nbsp;assure&nbsp;all clinical products meet the requirements for quality,&nbsp;safety&nbsp;and efficacy.&nbsp;</li>\n<li>Providing in-person and real-time manufacturing production support&nbsp;as&nbsp;needed.&nbsp;</li>\n<li>Collaborating with Supplier Quality and Manufacturing to evaluate change notifications or material non-conformances.&nbsp;&nbsp;</li>\n<li>Identifying&nbsp;continuous&nbsp;improvement opportunities and/or corrective actions to increase yield, maximize capacity, improve operational efficiency, reduce costs, and ensure safety while&nbsp;maintaining&nbsp;regulatory compliance in&nbsp;cross functional&nbsp;collaborations.&nbsp;</li>\n<li>Working closely with&nbsp;Quality&nbsp;department to ensure compliance with&nbsp;cGMP,&nbsp;ICH&nbsp;and FDA regulations.&nbsp;</li>\n<li>Serving as an organizational change agent and fostering an atmosphere of a questioning attitude, empowerment, and&nbsp;an error&nbsp;prevention/continuous improvement mindset.&nbsp;</li>\n<li>Performing such other duties as may be assigned to you from time to time.</li>\n"},{"text":"Requirements","content":"\n<li>Bachelor’s degree&nbsp;and&nbsp;2+ years of hands-on cGMP biologics manufacturing experience in pharmaceutical/biotech industry&nbsp;preferred, or equivalent combination of degree/experience.&nbsp;</li>\n<li>A minimum of 1&nbsp;year&nbsp;experience in adherent cell culture.&nbsp;Additional&nbsp;experience&nbsp;with&nbsp;cells in suspension is a plus.&nbsp;</li>\n<li>Experience with writing/revising&nbsp;technical documents&nbsp;is&nbsp;required&nbsp;(SOPs, Forms, Batch Records,&nbsp;etc).&nbsp;</li>\n<li>Previous&nbsp;experience with,&nbsp;or&nbsp;knowledge/understanding&nbsp;of,&nbsp;various&nbsp;quality events&nbsp;is&nbsp;required&nbsp;(Deviations, CAPAs, Change Controls&nbsp;etc).&nbsp;&nbsp;</li>\n<li>Deep understanding of&nbsp;cell culture and ability to troubleshoot common&nbsp;processing issues.&nbsp;</li>\n<li>Experience with scale-up of cell therapy processes&nbsp;and closed manufacturing systems preferred.&nbsp;&nbsp;</li>\n<li>Ability to collect and&nbsp;assist&nbsp;in the&nbsp;analyzation/trending of&nbsp;data and information to&nbsp;determine&nbsp;paths for process improvement and potential root cause.&nbsp;</li>\n<li>Demonstrates technical&nbsp;proficiency, scientific creativity, problem-solving skills, strong GMP&nbsp;principles&nbsp;and collaboration with others.&nbsp;</li>\n<li>Must have full working knowledge of cGMP regulations.&nbsp;</li>\n<li>Exceptional communication, presentation,&nbsp;and interpersonal skills.&nbsp;</li>\n<li>Strong Microsoft Word and Excel skills.&nbsp;</li>\n<li>Ability to work in a dynamic environment,&nbsp;multi-task,&nbsp;and&nbsp;meet aggressive deadlines.&nbsp;</li>\n<li>Ability to work independently, as well as work on larger cross-department projects&nbsp;as a team.&nbsp;</li>\n"},{"text":"Work Environment & Physical Demands","content":"\n<li>Professional GMP facility environment with controlled conditions.</li>\n<li>Ability to sit or stand for extended periods during training and operations.</li>\n<li>Occasional lifting of materials or equipment up to 40 pounds.</li>\n<li>Willingness to work inside an ISO7 cleanroom when supporting manufacturing operations.</li>\n<li>Compliance with gowning procedures and cleanroom protocols for aseptic activities.</li>\n"}],"salaryRange":{"min":72500,"max":87500,"currency":"USD","interval":"per-year-salary"},"text":"MSAT Associate 2","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div><span style=\"font-size: 10.5pt;\">The MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or&nbsp;biologics&nbsp;manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities.&nbsp;</span></div>\n<div>&nbsp;</div>\n<div><span style=\"font-size: 10.5pt;\">In this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations.&nbsp;</span></div>","descriptionBodyPlain":"The MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or biologics manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities. \n \nIn this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations. \n","hostedUrl":"https://jobs.lever.co/capricor/1b1ec559-3f4b-46c9-89a4-feaa9561e828","applyUrl":"https://jobs.lever.co/capricor/1b1ec559-3f4b-46c9-89a4-feaa9561e828/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"MSAT","allLocations":["San Diego, CA"]},"createdAt":1778104039471,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nAs an MSAT Training Specialist II/III at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>As an <strong>MSAT Training Specialist II/III</strong> at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development.</div>","id":"366071a4-728b-444f-901c-568540200836","lists":[{"text":"Responsibilities","content":"\n<li>Develop and deliver training sessions on GMP cell culture manufacturing, cell counting, and aseptic techniques.</li>\n<li>Design and implement innovative training modules and programs to enhance engagement and retention.</li>\n<li>Collaborate with subject matter experts to align training materials with regulatory standards.</li>\n<li>Mentor and coach manufacturing personnel, fostering a culture of continuous growth and strict GMP adherence.</li>\n<li>Oversee the creation, review, and maintenance of SOPs, batch records, and technical documents for training and compliance.</li>\n<li>Lead investigations, interviews, root cause analyses, and impact assessments for deviations, CAPAs, and change controls.</li>\n<li>Manage the training lab, ensuring it is fully equipped, stocked, and prepared for all training activities.</li>\n<li>Partner with Quality Assurance, Manufacturing, and Regulatory Affairs to integrate training with operational and compliance workflows.</li>\n<li>Monitor and evaluate training effectiveness using feedback, performance metrics, and audits to drive continuous improvement.</li>\n<li>Stay current with industry trends, regulatory changes, and best practices.</li>\n"},{"text":"Requirements","content":"\n<li>Bachelor’s degree in a life science discipline (e.g., Biology, Biotechnology) or equivalent experience.&nbsp;</li>\n<li>3-7 years of experience with mammalian cell culture manufacturing in a GMP environment.&nbsp;</li>\n<li>Proven expertise as a Subject Matter Expert or Trainer in GMP cell culture manufacturing.&nbsp;</li>\n<li>Extensive experience authoring and reviewing SOPs, batch records, and technical documents.</li>\n<li>Advanced knowledge of aseptic techniques, cell counting, and GMP production methods.</li>\n<li>Communication and presentation skills for diverse audiences.</li>\n<li>Exceptional communication skills and attention to detail for training materials and records.</li>\n<li>Ability to work independently and in a team in a dynamic setting.</li>\n<li>Experience with cleanroom operations and gowning procedures preferred.</li>\n<li>Knowledge of cell therapy manufacturing processes preferred.&nbsp;</li>\n"},{"text":"Work Environment & Physical Demands","content":"\n<li>Primarily laboratory-based with required time in GMP cleanroom environments addressing training and documentation.</li>\n<li>Requires prolonged periods of standing, computer use for training materials, and gowning for cleanroom work.</li>\n<li>May involve lifting materials or equipment up to 20 pounds.&nbsp;</li>\n<li>Ability to navigate laboratory and GMP environments for training and oversight.&nbsp;</li>\n"}],"salaryRange":{"min":75000,"max":95000,"currency":"USD","interval":"per-year-salary"},"text":"MSAT Training Specialist II/III","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>As an <strong>MSAT Training Specialist II/III</strong> at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development.</div>","descriptionBodyPlain":"As an MSAT Training Specialist II/III at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development.\n","hostedUrl":"https://jobs.lever.co/capricor/366071a4-728b-444f-901c-568540200836","applyUrl":"https://jobs.lever.co/capricor/366071a4-728b-444f-901c-568540200836/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (non-exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"General Administration","allLocations":["San Diego, CA"]},"createdAt":1777498920212,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies.  \nThis individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<p>The Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies. &nbsp;</p>\n<p>This individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace.&nbsp;</p>\n</div>","id":"9529613a-6d12-4f3b-8006-6aad4813db66","lists":[{"text":"Responsibilities","content":"<div>\n<div>\n<div>\n<p><strong><span data-contrast=\"auto\">Workplace Operations&nbsp;</span><span data-ccp-props=\"{&quot;335559685&quot;:0}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Conduct daily walkthroughs of office and&nbsp;common areas&nbsp;to ensure the workplace is clean, safe, and functioning properly.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Monitor restrooms, breakrooms, conference rooms, and shared spaces for cleanliness and supply levels.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ensure hallways, exits, and doorways&nbsp;remain&nbsp;clear and compliant with safety standards.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Report or coordinate resolution of maintenance or facility issues (lighting, plumbing, furniture, etc.).&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Submit and track facilities or janitorial service requests.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><strong><span data-contrast=\"auto\">Visitor &amp; Badge Management&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ensure all visitors follow company check-in procedures.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Support reception or front desk operations as needed.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Coordinate temporary badges or access requests.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><strong><span data-contrast=\"auto\">&nbsp;Parking &amp; Site Coordination&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"10\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Monitor company parking areas to ensure spaces are used appropriately.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"10\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Distribute parking passes when needed.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"10\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Address parking issues or coordinate with building management when necessary.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><strong><span data-contrast=\"auto\">&nbsp;</span><span data-contrast=\"auto\">Workplace Experience</span><span data-contrast=\"auto\">&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"11\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Serve as a visible and approachable point of contact for employees&nbsp;regarding&nbsp;workplace needs.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"11\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Assist&nbsp;with room setups, small internal events, or meetings.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"11\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Support onboarding&nbsp;logistics&nbsp;(workspace readiness, badge coordination, etc.).&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"11\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Help&nbsp;maintain&nbsp;an organized, welcoming office environment.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><strong><span data-contrast=\"auto\">&nbsp;Safety &amp; Compliance&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"13\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ensure fire exits, safety doors, and emergency routes&nbsp;remain&nbsp;unobstructed.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"13\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Escalate safety concerns promptly to leadership or facilities teams.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"13\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Support workplace policies&nbsp;regarding&nbsp;access control, safety, and shared space usage.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><strong><span data-contrast=\"auto\">&nbsp;</span><span data-contrast=\"auto\">Facilities Coordination&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></strong></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">&nbsp;Work with janitorial, maintenance, and building management teams to resolve issues.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Track recurring workplace needs and escalate trends when necessary.&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"},{"text":"Requirements","content":"<div>\n<div>\n<p><span data-contrast=\"auto\"><strong>Required</strong>&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">2+&nbsp;years experience&nbsp;in workplace operations, facilities support, office management, or a similar role&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Strong attention to detail and ability to notice issues before they become problems</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Excellent communication and customer service skills&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to work independently and prioritize tasks&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Comfortable working in a highly visible, employee-facing role&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to walk the facility&nbsp;frequently&nbsp;throughout the day&nbsp;</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"}],"salaryRange":{"min":27,"max":33,"currency":"USD","interval":"per-hour-wage"},"text":"Operations Coordinator","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<p>The Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies. &nbsp;</p>\n<p>This individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace.&nbsp;</p>\n</div>","descriptionBodyPlain":"The Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies.  \nThis individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace. \n","hostedUrl":"https://jobs.lever.co/capricor/9529613a-6d12-4f3b-8006-6aad4813db66","applyUrl":"https://jobs.lever.co/capricor/9529613a-6d12-4f3b-8006-6aad4813db66/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Commercial","allLocations":["San Diego, CA"]},"createdAt":1778727266969,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThis position will drive disciplined execution, operational readiness, and process excellence across Capricor’s commercial launch program. This role sits at the center of cross‑functional coordination—ensuring teams are aligned, risks are surfaced early, timelines are maintained, and launch-critical processes are mapped, optimized, and repeatable.\nThe ideal candidate brings experience supporting biotech/pharma commercial launches, paired with strong program management, operational excellence, and process‑improvement capabilities. This role is designed for someone who thrives in structured planning, cross‑functional orchestration, and building scalable frameworks in a fast‑moving, high‑growth environment.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>This position will drive disciplined execution, operational readiness, and process excellence across Capricor’s commercial launch program. This role sits at the center of cross‑functional coordination—ensuring teams are aligned, risks are surfaced early, timelines are maintained, and launch-critical processes are mapped, optimized, and repeatable.</div>\n<p>The ideal candidate brings experience supporting biotech/pharma commercial launches, paired with strong program management, operational excellence, and process‑improvement capabilities. This role is designed for someone who thrives in structured planning, cross‑functional orchestration, and building scalable frameworks in a fast‑moving, high‑growth environment.</p>","id":"43a64526-b7d9-44db-840d-451919029600","lists":[{"text":"Responsibilities","content":"<div>\n<p><strong>Commercial Launch Program Management</strong></p>\n<ul type=\"disc\">\n<li>Maintain the integrated <strong>commercial launch plan</strong>, tracking timelines, dependencies, and critical-path activities across Commercial, Medical, Market Access, Patient Services, Supply Chain, Quality, and Finance.</li>\n<li>Drive cross‑functional launch meetings: set agendas, capture decisions, track action items, and ensure accountable follow‑through.</li>\n<li>Prepare materials for commercial readiness reviews, governance meetings, and executive updates.</li>\n\n<p><strong>Operational Excellence &amp; Process Optimization</strong></p>\n<ul type=\"disc\">\n<li>Map, document, and optimize cross‑functional launch processes, identifying bottlenecks and opportunities for standardization.</li>\n<li>Build and maintain <strong>repeatable operating mechanisms</strong> (templates, trackers, dashboards, workflows, RACI matrices).</li>\n<li>Support continuous improvement by introducing tools, metrics, and operational discipline to strengthen execution quality.</li>\n\n<p><strong>Risk Management &amp; Governance</strong></p>\n<ul type=\"disc\">\n<li>Identify and mitigate risks, dependencies, and resource constraints impacting launch readiness.</li>\n<li>Ensure alignment between functional plans and enterprise‑level objectives, escalating issues when necessary.</li>\n<li>Maintain structured documentation (decision logs, RAID logs, governance summaries) to ensure transparency.</li>\n\n<p><strong>Cross‑Functional Alignment &amp; Communication</strong></p>\n<ul type=\"disc\">\n<li>Translate high‑level strategic goals into executable workplans with clear owners, timelines, and measurable outcomes.</li>\n<li>Serve as the central coordinator connecting Commercial with supporting functions (Regulatory, Quality, Supply Chain, Medical Affairs, Finance).</li>\n<li>Enable consistent communication and ensure all teams have access to up‑to‑date timelines, plans, and reference materials.</li>\n\n<p><strong>Post‑Launch Optimization</strong></p>\n<ul type=\"disc\">\n<li>Support post‑launch retrospectives by gathering lessons learned and integrating improvements into future launch frameworks.</li>\n<li>Partner with functional leads to refine SOPs, playbooks, and operational processes for future programs.</li>\n\n</ul></ul></ul></ul></ul></div>"},{"text":"Requirements","content":"<div>\n<ul type=\"disc\">\n<li>Bachelor’s degree required; PMP, CAPM, Lean/Six Sigma, or program management training a strong plus.</li>\n<li><strong>3–5+ years of experience supporting biotech/pharma commercial launches</strong> (required).</li>\n<li>Experience in <strong>program management, operational excellence, or process optimization</strong> within life sciences.</li>\n<li>Strong ability to manage multiple parallel workstreams, synthesize complex information, and drive structured execution.</li>\n<li>Excellent communication, facilitation, and follow‑through skills; effective at influencing without authority.</li>\n<li>Proficiency with project management and workflow tools (Smartsheet, MS Project, Asana, Monday.com, Miro, etc.).</li>\n<li>Comfort working in a dynamic, lean biotech environment with evolving priorities and accelerated timelines.</li>\n\n</ul></div>"},{"text":"Work Environment & Physical Demands","content":"<ul type=\"disc\">\n<li>Office work environment with occasional travel for planning sessions and cross‑functional workshops.</li>\n<li>Ability to manage multiple priorities with high attention to detail and strong organizational discipline.</li>\n</ul>"}],"salaryRange":{"min":100000,"max":140000,"currency":"USD","interval":"per-year-salary"},"text":"Program Manager, Commercial Operations","country":"US","workplaceType":"hybrid","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>This position will drive disciplined execution, operational readiness, and process excellence across Capricor&rsquo;s commercial launch program. This role sits at the center of cross‑functional coordination&mdash;ensuring teams are aligned, risks are surfaced early, timelines are maintained, and launch-critical processes are mapped, optimized, and repeatable.</div>\n<p>The ideal candidate brings experience supporting biotech/pharma commercial launches, paired with strong program management, operational excellence, and process‑improvement capabilities. This role is designed for someone who thrives in structured planning, cross‑functional orchestration, and building scalable frameworks in a fast‑moving, high‑growth environment.</p>","descriptionBodyPlain":"This position will drive disciplined execution, operational readiness, and process excellence across Capricor’s commercial launch program. This role sits at the center of cross‑functional coordination—ensuring teams are aligned, risks are surfaced early, timelines are maintained, and launch-critical processes are mapped, optimized, and repeatable.\nThe ideal candidate brings experience supporting biotech/pharma commercial launches, paired with strong program management, operational excellence, and process‑improvement capabilities. This role is designed for someone who thrives in structured planning, cross‑functional orchestration, and building scalable frameworks in a fast‑moving, high‑growth environment.\n","hostedUrl":"https://jobs.lever.co/capricor/43a64526-b7d9-44db-840d-451919029600","applyUrl":"https://jobs.lever.co/capricor/43a64526-b7d9-44db-840d-451919029600/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Assurance","allLocations":["San Diego, CA"]},"createdAt":1761582806046,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nWe are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>We are seeking a <strong>Quality Assurance Associate II </strong>to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.</div>","id":"7a6b869f-2b42-4e9e-a40f-5ba89d556a12","lists":[{"text":"Responsibilities","content":"\n<li>Assist in batch record review and disposition for clinical product manufacturing, including label issuance, product packaging, and shipping activities.</li>\n<li>Support the issuance, tracking, and archiving of controlled documentation in compliance with&nbsp;GxP&nbsp;(GLP/GCP/GMP) regulations.&nbsp;</li>\n<li>Maintain and manage controlled records, including batch/test records, logs, reports, and quality management documentation.&nbsp;</li>\n<li>Assist&nbsp;in preparing materials for internal audits and ensuring&nbsp;documentation&nbsp;readiness for regulatory inspections.&nbsp;</li>\n<li>Help process and track training records to ensure company-wide&nbsp;GxP&nbsp;compliance.&nbsp;</li>\n<li>Participate in the review and release of incoming materials&nbsp;in accordance with&nbsp;company standards.&nbsp;</li>\n<li>Support controlled label issuance, including inventory tracking and updating lot numbers.&nbsp;</li>\n<li>Collaborate with senior team members to improve and implement quality management systems and training programs.&nbsp;</li>\n<li>Assist&nbsp;in preparing reports and documentation related to deviations, corrective actions, and&nbsp;change&nbsp;controls.&nbsp;</li>\n<li>Support the maintenance and management of documentation systems, both manual and electronic, ensuring&nbsp;timely&nbsp;and&nbsp;accurate&nbsp;record-keeping.&nbsp;</li>\n<li>Perform&nbsp;additional&nbsp;quality assurance tasks as assigned.&nbsp;</li>\n"},{"text":"Requirements","content":"\n<li>Bachelor’s degree in a relevant field (e.g., Biology, Biotechnology, or related discipline) or equivalent experience.&nbsp;</li>\n<li>0-3 years of experience in a regulated environment (e.g., cGMP, GLP, GCP).&nbsp;</li>\n<li>Familiarity with regulatory standards such as 21 CFR 210 and 211, ICH, ISO9001, and FDA guidelines preferred.&nbsp;</li>\n<li>Strong attention to detail and excellent organizational skills for managing documentation and records.&nbsp;</li>\n<li>Proficiency&nbsp;in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with database systems.&nbsp;</li>\n<li>Strong written and verbal communication skills for effective collaboration and reporting.&nbsp;</li>\n<li>Ability to work independently and as part of a team in a dynamic, fast-paced environment.&nbsp;</li>\n<li>Comfortable gowning and working in classified areas as&nbsp;required.&nbsp;</li>\n"},{"text":"Work Environment / Physical Demands ","content":"\n<li>Primarily office-based with occasional time in GMP cleanroom environments for documentation and oversight tasks.&nbsp;</li>\n<li>Requires prolonged periods of computer use for documentation and record&nbsp;management, and&nbsp;gowning for cleanroom work.&nbsp;</li>\n<li>May involve lifting materials or equipment up to 20 pounds.&nbsp;</li>\n<li>Ability to navigate&nbsp;office&nbsp;and&nbsp;classified&nbsp;GMP environments for quality assurance activities.&nbsp;</li>\n"}],"salaryRange":{"currency":"USD","interval":"per-year-salary","min":70305,"max":82000},"text":"Quality Assurance Associate II","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>We are seeking a <strong>Quality Assurance Associate II </strong>to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.</div>","descriptionBodyPlain":"We are seeking a Quality Assurance Associate II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.\n","hostedUrl":"https://jobs.lever.co/capricor/7a6b869f-2b42-4e9e-a40f-5ba89d556a12","applyUrl":"https://jobs.lever.co/capricor/7a6b869f-2b42-4e9e-a40f-5ba89d556a12/apply"},{"additionalPlain":"","additional":"<div>\n<div><strong>Why Capricor?</strong></div>\n<div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div>\n<div>&nbsp;</div>\n<div><strong>Come Work With Us!</strong></div>\n<div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div>\n<div>&nbsp;</div>\n<div><em>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</em></div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div>&nbsp;</div>\n<div><strong>Notice to Recruiting Agencies</strong></div>\n<div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>\n</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego - SD3","team":"Quality Compliance","allLocations":["San Diego - SD3"]},"createdAt":1779214079346,"descriptionPlain":"","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>\n<div>&nbsp;</div>\n<div><span data-contrast=\"auto\">We are seeking an&nbsp;individual&nbsp;to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures. The ideal candidate brings hands-on GMP/GxP auditing experience within the life sciences industry and partners cross-functionally to drive continuous improvement and a strong culture of compliance.</span><span data-ccp-props=\"{}\">&nbsp;</span></div>","id":"5b0afe94-7e55-4295-b596-2e5cdaad8711","lists":[{"text":"Key Responsibilities ","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Plan, execute, and report on internal audits of GxP processes (e.g., GMP manufacturing, QC, validation, laboratories, supply chain).</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Lead or support supplier/vendor audits and monitor ongoing supplier performance.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Prepare detailed audit agendas, checklists, and sampling strategies aligned with risk and compliance priorities.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Document findings clearly; issue audit reports with classifications, evidence, and actionable recommendations.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Track and verify effectiveness of CAPAs (Corrective and Preventive Actions) and drive timely closure.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Support inspection readiness activities and host/liaise during regulatory inspections (e.g., FDA, EMA, MHRA).</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\"><span data-ccp-parastyle=\"List Bullet\">Perform gap assessments against current regulations and industry standards; propose&nbsp;</span><span data-ccp-parastyle=\"List Bullet\">reasonable</span><span data-ccp-parastyle=\"List Bullet\">&nbsp;improvements.</span></span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"8\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Collaborate with QA/QC, Manufacturing, Regulatory, Supply Chain, and IT to strengthen quality systems.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"9\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Maintain audit schedules, metrics, and dashboards; communicate status to stakeholders and management.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"10\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Contribute to policy/SOP development, training, and continuous improvement initiatives.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"},{"text":"Minimum Qualifications ","content":"<div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"11\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Bachelor's degree in a scientific or technical field (e.g., Chemistry, Biology, Engineering) or equivalent experience.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"12\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">1-2 years of auditing experience within biopharma, biotech, medical devices, or related regulated industry.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"13\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Working knowledge of FDA 21 CFR Parts 210/211, ICH Q-series, EU GMP, and GDP principles.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"14\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Experience performing audits against quality system elements (Deviation, CAPA, Change Control, Training, Document Control).</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"15\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Strong technical writing skills and attention to detail; able to produce clear, evidence-based audit reports.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"16\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Proficiency with risk-based auditing, root cause analysis, and CAPA effectiveness verification.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"17\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Excellent communication and stakeholder management skills; comfortable engaging at all levels.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"},{"text":"Preferred Qualifications ","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"18\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\"><span data-ccp-parastyle=\"List Bullet\">Certified Quality Auditor (CQA) – ASQ, or equivalent certification</span><span data-ccp-parastyle=\"List Bullet\">.</span></span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"19\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Experience auditing CMOs/CDMOs and complex supply chains.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"20\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\"><span data-ccp-parastyle=\"List Bullet\">Background with data integrity, CS</span><span data-ccp-parastyle=\"List Bullet\">V</span><span data-ccp-parastyle=\"List Bullet\">, Annex 11, and Part 11 assessments.</span></span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"21\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-ccp-parastyle=\"List Bullet\">Exposure to biologics, cell &amp; gene therapy, aseptic processing, or sterile manufacturing.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"1\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:360,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;singleLevel&quot;}\" data-aria-posinset=\"22\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\"><span data-ccp-parastyle=\"List Bullet\">Knowledge of ISO 9001/13485</span><span data-ccp-parastyle=\"List Bullet\">, 21 CFR 210/211,&nbsp;</span><span data-ccp-parastyle=\"List Bullet\">and pharmacovigilance quality systems (as applicable).</span></span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"}],"salaryRange":{"min":70000,"max":82000,"currency":"USD","interval":"per-year-salary"},"text":"Quality Compliance Associate I/II","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX&trade; exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>\n<div>&nbsp;</div>\n<div><span xml:lang=\"EN-US\" data-contrast=\"auto\">We are seeking an&nbsp;individual&nbsp;to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures. The ideal candidate brings hands-on GMP/GxP auditing experience within the life sciences industry and partners cross-functionally to drive continuous improvement and a strong culture of compliance.</span><span data-ccp-props=\"{}\">&nbsp;</span></div>","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/5b0afe94-7e55-4295-b596-2e5cdaad8711","applyUrl":"https://jobs.lever.co/capricor/5b0afe94-7e55-4295-b596-2e5cdaad8711/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Control","allLocations":["San Diego, CA"]},"createdAt":1779486723320,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, performing analytical studies to evaluate assay performance, and supporting troubleshooting and optimization of analytical methods used in QC testing. \nThis position plays an important role in ensuring the reliability and consistency of QC assays by supporting the generation, characterization, and maintenance of assay controls. The individual will work closely with QC scientists and cross-functional teams to support assay performance monitoring and continuous improvement of analytical methods used across Capricor’s therapeutic programs. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<div>\n<p><span data-contrast=\"auto\">The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will&nbsp;be responsible for&nbsp;generating and&nbsp;maintaining&nbsp;positive and negative controls, performing analytical studies to evaluate assay performance, and supporting troubleshooting and optimization of analytical methods used in QC testing.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">This position plays&nbsp;an important role&nbsp;in ensuring the reliability and consistency of QC assays by supporting the generation, characterization, and maintenance of assay controls. The individual will work closely with QC scientists and cross-functional teams to support assay performance monitoring and continuous improvement of analytical methods used across&nbsp;Capricor’s&nbsp;therapeutic programs.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>","id":"e3157e36-ccf3-4964-a44d-d6548f3805f0","lists":[{"text":"Responsibilities","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Generate, prepare, and&nbsp;maintain&nbsp;positive and negative control materials used in QC analytical assays.</span></li>\n<li><span data-contrast=\"auto\">Support the qualification and characterization of control materials to ensure suitability for routine QC testing.</span></li>\n<li><span data-contrast=\"auto\">Execute analytical assays to support control evaluation, assay troubleshooting, and assay optimization studies.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n<li><span data-contrast=\"auto\">Perform laboratory activities related to control generation, characterization, and assay performance evaluation.</span></li>\n<li><span data-contrast=\"auto\">Maintain inventory, traceability, and documentation of assay control materials used across QC testing programs.</span></li>\n<li><span data-contrast=\"auto\">Analyze experimental data, summarize results, and document findings in accordance with GMP and data integrity requirements.</span></li>\n<li><span data-contrast=\"auto\">Document all laboratory work in GMP-compliant systems including laboratory notebooks, controlled forms, and electronic records.</span></li>\n<li><span data-contrast=\"auto\">Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, and control qualification records.</span></li>\n<li><span data-contrast=\"auto\">Assist with investigations related to assay performance including deviations, OOS/OOT events, and atypical assay results.</span></li>\n<li><span data-contrast=\"auto\">Collaborate with QC scientists and cross-functional teams including Analytical Development, Process Development, Manufacturing, and Quality to support assay readiness and continuous improvement initiatives.</span></li>\n<li><span data-contrast=\"auto\">Manage multiple laboratory assignments and testing priorities to meet project timelines and QC operational needs.</span></li>\n<li><span data-contrast=\"auto\">Perform additional QC duties as assigned.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"},{"text":"Required Qualifications (Must‑Haves)","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Bachelor’s degree in Biological Sciences, Biochemistry, Molecular Biology, or&nbsp;a related&nbsp;discipline.</span></li>\n<li><span data-contrast=\"auto\">2+ years of laboratory experience in biotechnology, pharmaceutical, or GMP-regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Hands-on experience performing analytical assays such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience preparing or maintaining assay controls or reference materials.</span></li>\n<li><span data-contrast=\"auto\">Strong laboratory documentation practices and familiarity with GMP and data integrity expectations.</span></li>\n<li><span data-contrast=\"auto\">Ability to analyze data and communicate findings clearly.</span></li>\n<li><span data-contrast=\"auto\">Ability to work independently and manage multiple assignments in a laboratory environment.</span></li>\n<li><span data-contrast=\"auto\">Strong organizational and time management skills.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"},{"text":"Preferred Qualifications (Nice‑to‑Haves)","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Experience supporting analytical studies related to assay performance or assay optimization.</span></li>\n<li><span data-contrast=\"auto\">Experience working with mammalian cell culture or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting method qualification or assay performance monitoring activities.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting deviations, investigations, or technical reports in regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Experience working with cell therapy, biologics, or exosome-based products.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"},{"text":"Work Environment & Physical Requirements","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Laboratory-based role&nbsp;requiring&nbsp;routine bench work.</span></li>\n<li><span data-contrast=\"auto\">Work involves analytical instrumentation, laboratory documentation, and computer-based data analysis.</span></li>\n<li><span data-contrast=\"auto\">Ability to lift up to 20 pounds.</span></li>\n<li><span data-contrast=\"auto\">Occasional participation in cross-functional meetings and technical discussions.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"}],"salaryRange":{"min":75000,"max":87000,"currency":"USD","interval":"per-year-salary"},"text":"Quality Control Associate II, Controls","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<div>\n<p><span xml:lang=\"EN-US\" data-contrast=\"auto\">The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will&nbsp;be responsible for&nbsp;generating and&nbsp;maintaining&nbsp;positive and negative controls, performing analytical studies to evaluate assay performance, and supporting troubleshooting and optimization of analytical methods used in QC testing.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span xml:lang=\"EN-US\" data-contrast=\"auto\">This position plays&nbsp;an important role&nbsp;in ensuring the reliability and consistency of QC assays by supporting the generation, characterization, and maintenance of assay controls. The individual will work closely with QC scientists and cross-functional teams to support assay performance monitoring and continuous improvement of analytical methods used across&nbsp;Capricor&rsquo;s&nbsp;therapeutic programs.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>","descriptionBodyPlain":"The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, performing analytical studies to evaluate assay performance, and supporting troubleshooting and optimization of analytical methods used in QC testing. \nThis position plays an important role in ensuring the reliability and consistency of QC assays by supporting the generation, characterization, and maintenance of assay controls. The individual will work closely with QC scientists and cross-functional teams to support assay performance monitoring and continuous improvement of analytical methods used across Capricor’s therapeutic programs. \n","hostedUrl":"https://jobs.lever.co/capricor/e3157e36-ccf3-4964-a44d-d6548f3805f0","applyUrl":"https://jobs.lever.co/capricor/e3157e36-ccf3-4964-a44d-d6548f3805f0/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Control","allLocations":["San Diego, CA"]},"createdAt":1778690720416,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Quality Control Scientist will be a key contributor to Capricor’s mission of delivering innovative cell and regenerative therapies, ensuring the highest standards of product quality at our San Diego facility. This lab-based role is critical in advancing our quality control framework by optimizing and validating analytical methods, facilitating seamless technology transfers, and driving continuous improvement initiatives. The scientist will work closely with cross-functional teams to support the development and commercialization of novel therapies, including cell-based products and exosomes, while ensuring compliance with stringent regulatory standards. This position offers a unique opportunity to shape phase-appropriate QC strategies, implement cutting-edge technologies, and directly impact patient outcomes through robust quality assurance.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<p>The Quality Control Scientist will be a key contributor to Capricor’s mission of delivering innovative cell and regenerative therapies, ensuring the highest standards of product quality at our San Diego facility. This lab-based role is critical in advancing our quality control framework by optimizing and validating analytical methods, facilitating seamless technology transfers, and driving continuous improvement initiatives. The scientist will work closely with cross-functional teams to support the development and commercialization of novel therapies, including cell-based products and exosomes, while ensuring compliance with stringent regulatory standards. This position offers a unique opportunity to shape phase-appropriate QC strategies, implement cutting-edge technologies, and directly impact patient outcomes through robust quality assurance.</p>\n</div>","id":"243f4f96-e314-4d45-a7e4-1aeab3ff05f0","lists":[{"text":"Responsibilities","content":"\n<li>Optimize and troubleshoot QC methods to enhance performance, consistency, and efficiency.</li>\n<li>Support method qualification, validation, and lifecycle management per regulatory expectations (ICH, USP, FDA).</li>\n<li>Perform data trending and analysis to monitor assay performance and detect method variability or drift.</li>\n<li>Collaborate with Analytical Development for seamless method transfers and onboarding of new assays into the QC laboratory.</li>\n<li>Draft and review method SOPs, validation protocols/reports, and technical documentation.</li>\n<li>Contribute to investigations, CAPAs, and continuous improvement initiatives within the QC function.</li>\n<li>Evaluate and implement new technologies or instrumentation to improve assay robustness and throughput.</li>\n<li>Provide technical documentation and SME input for regulatory inspections and audits.</li>\n<li>Participate in risk assessments, gap analyses, and change control activities related to QC methods.</li>\n<li>Train QC analysts on new or optimized assays to ensure consistent and compliant execution.</li>\n<li>Author and review technical reports, method development summaries, and QC method lifecycle documents.</li>\n<li>Maintain GMP documentation and laboratory practices with a strong lab-based presence.</li>\n"},{"text":"Required Qualifications (Must‑Haves)","content":"\n<li>Bachelor’s degree in a relevant Biological Science discipline (Master’s or Ph.D. preferred).</li>\n<li>7+ years of experience in a GMP Quality Control laboratory or GMP/GLP setting.</li>\n<li>In-depth knowledge of FDA regulations, ICH guidelines, USP standards, and cGMP requirements for cell therapy or biologics.</li>\n<li>Hands-on experience with laboratory methods including flow cytometry, Real-Time PCR, DNA isolation, ELISA, bioactivity assays, and sequencing.</li>\n<li>Proven expertise in method qualification and validation.</li>\n<li>Ability to independently perform laboratory analysis, troubleshoot, and improve methods.</li>\n<li>Demonstrated history of successful, independent laboratory work.</li>\n<li>Excellent communication skills and ability to collaborate effectively in a team environment.</li>\n"},{"text":"Work Environment & Physical Requirements","content":"\n<li>Must be able to sit or stand for extended periods, move around the facility, communicate effectively, and lift/carry up to 40 lbs.</li>\n<li>Ability to gown and work in a classified area as required.</li>\n"}],"salaryRange":{"min":100000,"max":115000,"currency":"USD","interval":"per-year-salary"},"text":"Quality Control Scientist","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<p>The Quality Control Scientist will be a key contributor to Capricor&rsquo;s mission of delivering innovative cell and regenerative therapies, ensuring the highest standards of product quality at our San Diego facility. This lab-based role is critical in advancing our quality control framework by optimizing and validating analytical methods, facilitating seamless technology transfers, and driving continuous improvement initiatives. The scientist will work closely with cross-functional teams to support the development and commercialization of novel therapies, including cell-based products and exosomes, while ensuring compliance with stringent regulatory standards. This position offers a unique opportunity to shape phase-appropriate QC strategies, implement cutting-edge technologies, and directly impact patient outcomes through robust quality assurance.</p>\n</div>","descriptionBodyPlain":"The Quality Control Scientist will be a key contributor to Capricor’s mission of delivering innovative cell and regenerative therapies, ensuring the highest standards of product quality at our San Diego facility. This lab-based role is critical in advancing our quality control framework by optimizing and validating analytical methods, facilitating seamless technology transfers, and driving continuous improvement initiatives. The scientist will work closely with cross-functional teams to support the development and commercialization of novel therapies, including cell-based products and exosomes, while ensuring compliance with stringent regulatory standards. This position offers a unique opportunity to shape phase-appropriate QC strategies, implement cutting-edge technologies, and directly impact patient outcomes through robust quality assurance.\n","hostedUrl":"https://jobs.lever.co/capricor/243f4f96-e314-4d45-a7e4-1aeab3ff05f0","applyUrl":"https://jobs.lever.co/capricor/243f4f96-e314-4d45-a7e4-1aeab3ff05f0/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Control","allLocations":["San Diego, CA"]},"createdAt":1779486493609,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing. \n \nThis position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across Capricor’s therapeutic programs. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing.&nbsp;</div>\n<div>&nbsp;</div>\n<div><span data-contrast=\"auto\">This position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across&nbsp;Capricor’s&nbsp;therapeutic programs.</span><span data-ccp-props=\"{}\">&nbsp;</span></div>","id":"ff4c8e8a-ce67-4736-b0e1-e2c552d8492d","lists":[{"text":"Responsibilities","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Lead the development, qualification, and maintenance of positive and negative control materials used in QC analytical assays.</span></li>\n<li><span data-contrast=\"auto\">Establish and oversee assay control strategies to ensure reliable assay performance and consistency across QC testing programs.</span></li>\n<li><span data-contrast=\"auto\">Serve as the scientific owner for control materials within the analytical lifecycle framework, including control generation, qualification, monitoring, and lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Design and execute analytical studies to evaluate assay performance, control suitability, assay robustness, and method reliability.</span></li>\n<li><span data-contrast=\"auto\">Provide scientific leadership for assay troubleshooting and optimization activities to improve assay robustness and reproducibility.</span></li>\n<li><span data-contrast=\"auto\">Evaluate assay performance trends and control performance data to identify opportunities for improving assay reliability.</span></li>\n<li><span data-contrast=\"auto\">Analyze experimental data, interpret results, and generate scientific reports, study summaries, and technical documentation.</span></li>\n<li><span data-contrast=\"auto\">Document experimental work and study outcomes in accordance with GMP and data integrity requirements.</span></li>\n<li><span data-contrast=\"auto\">Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, control qualification records, and analytical lifecycle documentation.</span></li>\n<li><span data-contrast=\"auto\">Support regulatory inspection readiness by ensuring analytical control strategies, documentation, and study records meet regulatory expectations.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n<li><span data-contrast=\"auto\">Provide scientific support for investigations including deviations, OOS/OOT events, and assay performance issues.</span></li>\n<li><span data-contrast=\"auto\">Collaborate with Analytical Development, Process Development, Manufacturing, and Quality teams to support assay lifecycle management and continuous improvement initiatives.</span></li>\n<li><span data-contrast=\"auto\">Manage multiple scientific projects and timelines to support QC laboratory priorities.</span></li>\n<li><span data-contrast=\"auto\">Perform additional QC duties as assigned.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"},{"text":"Required Qualifications (Must‑Haves)","content":"<div>\n\n<li><span data-contrast=\"auto\">Ph.D. in Biological Sciences, Biochemistry, Molecular Biology, Bioengineering, or&nbsp;a related&nbsp;discipline.</span></li>\n<li><span data-contrast=\"auto\">Strong background in primary cell culture and analytical assay development, troubleshooting, and experimental design.</span></li>\n<li><span data-contrast=\"auto\">Hands-on experience with analytical techniques such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.</span></li>\n<li><span data-contrast=\"auto\">Experience designing and executing analytical studies and interpreting experimental data.</span></li>\n<li><span data-contrast=\"auto\">Strong understanding of assay controls, assay performance monitoring, and analytical method lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Strong written and verbal communication skills with the ability to clearly summarize complex scientific findings.</span></li>\n<li><span data-contrast=\"auto\">Ability to work independently and manage multiple scientific projects in a fast-paced environment.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>"},{"text":"Preferred Qualifications (Nice‑to‑Haves)","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Experience working in GMP or regulated laboratory environments.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting analytical method qualification, validation, or lifecycle management.</span></li>\n<li><span data-contrast=\"auto\">Experience working with cell-based assays or mammalian cell culture systems.</span></li>\n<li><span data-contrast=\"auto\">Experience supporting deviations, assay investigations, or technical reports in regulated environments.</span></li>\n<li><span data-contrast=\"auto\">Experience with cell therapy, biologics, or exosome-based products.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"},{"text":"Work Environment & Physical Requirements","content":"<div>\n<div>\n\n<li><span data-contrast=\"auto\">Laboratory-based role&nbsp;requiring&nbsp;routine bench work.</span></li>\n<li><span data-contrast=\"auto\">Work involves analytical instrumentation, laboratory documentation, and computer-based data analysis.</span></li>\n<li><span data-contrast=\"auto\">Ability to lift up to 20 pounds.</span></li>\n<li><span data-contrast=\"auto\">Occasional participation in cross-functional meetings and technical discussions.</span><span data-ccp-props=\"{}\">&nbsp;</span></li>\n\n</div>\n</div>"}],"salaryRange":{"min":95000,"max":115000,"currency":"USD","interval":"per-year-salary"},"text":"Quality Control Scientist, Controls","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing.&nbsp;</div>\n<div>&nbsp;</div>\n<div><span xml:lang=\"EN-US\" data-contrast=\"auto\">This position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across&nbsp;Capricor&rsquo;s&nbsp;therapeutic programs.</span><span data-ccp-props=\"{}\">&nbsp;</span></div>","descriptionBodyPlain":"The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing. \n \nThis position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across Capricor’s therapeutic programs. \n","hostedUrl":"https://jobs.lever.co/capricor/ff4c8e8a-ce67-4736-b0e1-e2c552d8492d","applyUrl":"https://jobs.lever.co/capricor/ff4c8e8a-ce67-4736-b0e1-e2c552d8492d/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Control","allLocations":["San Diego, CA"]},"createdAt":1779486266883,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing. Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><p>The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing.&nbsp;Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.</p>","id":"918f1bc2-22ab-4149-bd7c-5fc3c9319ec9","lists":[{"text":"Responsibilities","content":"\n<li>Lead and support investigations related to deviations, OOS/OOT/invalid results, and CAPAs, ensuring thorough root cause analysis and clear documentation.</li>\n<li>Review QC data, laboratory records, and analytical results to assess product impact and ensure compliance with cGMP standards.</li>\n<li>Author and review SOPs, test methods, validation protocols/reports, and investigation summaries.</li>\n<li>Perform data trending and analysis to identify variability, shifts, or emerging risks in QC and product quality data.</li>\n<li>Support method lifecycle activities including qualification, validation, transfer, and periodic review in collaboration with Analytical Development.</li>\n<li>Provide technical oversight of QC methods to ensure they remain scientifically sound and fit for purpose.</li>\n<li>Contribute to change control activities and assess potential impact to product quality and method performance.</li>\n<li>Support maintenance of product specifications, including acceptance criteria and scientific justification.</li>\n<li>Participate in stability program activities, including data review and trending to support shelf-life determinations.</li>\n<li>Ensure accurate, complete, and compliant GMP documentation in alignment with data integrity (ALCOA+) principles.</li>\n<li>Support audits and regulatory inspections by preparing and reviewing technical documentation.</li>\n<li>Collaborate cross-functionally with QA, Manufacturing, and external partners to support product quality objectives.</li>\n<li>Contribute to quality risk assessments (ICH Q9), continuous improvement initiatives, and quality system enhancements.</li>\n"},{"text":"Required Qualifications (Must‑Haves)","content":"\n<li>Bachelor’s degree in Life Sciences, Biotechnology, or related field (advanced degree preferred).</li>\n<li>~5–8+ years of experience in GMP Quality Control, Quality Assurance, or related function within biotech or pharmaceutical industry.</li>\n<li>Strong knowledge of cGMP, FDA/EMA regulations, and ICH guidelines.</li>\n<li>Experience with deviation investigations, OOS/OOT, CAPAs, and change control processes.</li>\n<li>Strong technical writing, data analysis, and problem-solving skills.</li>\n<li>Working knowledge of analytical methods such as flow cytometry, PCR, ELISA, and bioassays.</li>\n<li>Excellent communication skills and ability to collaborate in a cross-functional environment.</li>\n<li>High attention to detail and commitment to quality and compliance.</li>\n"},{"text":"Work Environment & Physical Requirements","content":"\n<li>Primarily office-based with occasional presence in laboratory or manufacturing areas as needed.</li>\n<li>Ability to sit or stand for extended periods and move throughout the facility.</li>\n<li>Ability to gown and enter classified areas when required.</li>\n<li>Ability to lift and carry up to 40 lbs as needed.</li>\n"}],"salaryRange":{"min":75000,"max":95000,"currency":"USD","interval":"per-year-salary"},"text":"Quality Control Specialist, Analytical","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<p>The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing.&nbsp;Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.</p>","descriptionBodyPlain":"The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing. Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.\n","hostedUrl":"https://jobs.lever.co/capricor/918f1bc2-22ab-4149-bd7c-5fc3c9319ec9","applyUrl":"https://jobs.lever.co/capricor/918f1bc2-22ab-4149-bd7c-5fc3c9319ec9/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Research","allLocations":["San Diego, CA"]},"createdAt":1779484801023,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nWe are seeking a Science to join our Pre-Clinical team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>We are seeking a <strong>Science</strong> to join our <strong>Pre-Clinical</strong> team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.</div>","id":"eee342d7-9645-4e94-94f4-ae9fe3ff0e7e","lists":[{"text":"Responsibilities","content":"\n<li>Partner with the Principal Scientist and Director to provide preclinical expertise, including animal handling and study design.</li>\n<li>Plan, execute, and analyze in vivo and ex vivo studies to support program objectives.</li>\n<li>Perform cell-based assays and tissue analyses from in vivo studies; compile and report results.</li>\n<li>Conduct survival surgeries and establish rodent models using aseptic techniques.</li>\n<li>Develop, characterize, and implement new animal models to enhance pharmacology study effectiveness.</li>\n<li>Maintain detailed, audit-ready documentation of all studies to ensure data integrity and traceability.</li>\n<li>Optimize and implement best practices for in vivo research, including model selection, dosing strategies, and sample/data collection techniques.</li>\n<li>Ensure compliance with regulatory guidelines and ethical standards for all preclinical activities.</li>\n<li>Evaluate and integrate new technologies and platforms to improve study efficiency and quality.</li>\n<li>Perform and interpret preclinical imaging studies (e.g., IVIS).</li>\n<li>Contribute to a team culture that promotes continuous improvement, ownership, and inclusion.</li>\n"},{"text":"Minimum Requirements","content":"\n<li>Ph.D. in a relevant scientific discipline with expertise in nonclinical operations within drug discovery and development.</li>\n<li>Hands-on experience with cell biology techniques, including RNA/DNA extraction, PCR, Western blot, ELISA, and interventional assays for small molecules and biologics.</li>\n"},{"text":"Preferred Qualifications","content":"\n<li>2+ postdoc or industry experience</li>\n<li>Experience across diverse therapeutic modalities (small molecules, biologics, nucleic acid therapeutics, gene therapy).</li>\n<li>Familiarity with age-related disease models (inflammation, metabolic disorders, neurodegeneration, muscle atrophy, bone/joint deficits).</li>\n<li>Experience with metabolic chambers, behavioral assays, and related data analysis.</li>\n"},{"text":"Work Environment and Physical Demands","content":"\n<li>On-site laboratory environment with routine handling of animals and biological samples.</li>\n<li>Prolonged periods of standing and performing surgical or technical procedures.</li>\n<li>Ability to lift laboratory materials up to 20 pounds.</li>\n"}],"salaryRange":{"min":95000,"max":115000,"currency":"USD","interval":"per-year-salary"},"text":"Scientist – Preclinical Team","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>We are seeking a <strong>Science</strong> to join our <strong>Pre-Clinical</strong> team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.</div>","descriptionBodyPlain":"We are seeking a Science to join our Pre-Clinical team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.\n","hostedUrl":"https://jobs.lever.co/capricor/eee342d7-9645-4e94-94f4-ae9fe3ff0e7e","applyUrl":"https://jobs.lever.co/capricor/eee342d7-9645-4e94-94f4-ae9fe3ff0e7e/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"Remote","team":"Medical Affairs","allLocations":["Remote"]},"createdAt":1778792186459,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nCapricor is seeking Senior Director of Medical Affairs with deep expertise in biotechnology, ideally in rare diseases or cell therapies. This position will play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. This individual will define the roadmap for our scientific narrative, drive clinical scientific messaging, foster key relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), and patient advocacy groups in the DMD and BMD communities, and ensure high-integrity, compliant processes for stakeholder engagement. This new headcount position supports our major milestone of positive Phase 3 results and continued advancement of deramiocel. They will lead cross-functional efforts to bridge clinical development with commercialization readiness, fostering deep relationships and evidence generation strategies necessary to drive program success and ongoing medical excellence.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>Capricor is seeking Senior Director of Medical Affairs with deep expertise in biotechnology, ideally in rare diseases or cell therapies. This position will play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. This individual will define the roadmap for our scientific narrative, drive clinical scientific messaging, foster key relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), and patient advocacy groups in the DMD and BMD communities, and ensure high-integrity, compliant processes for stakeholder engagement. This new headcount position supports our major milestone of positive Phase 3 results and continued advancement of deramiocel. They will lead cross-functional efforts to bridge clinical development with commercialization readiness, fostering deep relationships and evidence generation strategies necessary to drive program success and ongoing medical excellence.</div>","id":"079eb323-62ae-415b-9d52-fac80496067a","lists":[{"text":"Responsibilities","content":"\n<li>Develop and execute medical affairs strategies aligned with company goals, including evidence generation, scientific exchange, and medical input into cross-functional teams.</li>\n<li>Build and maintain strong relationships with HCPs, KOLs, and patient advocacy organizations in DMD, Becker muscular dystrophy (BMD), and related fields through local, national, and international meetings, 1:1 site visits, and advisory boards.</li>\n<li>Collaborate with the CMO to establish high-integrity, compliant processes for HCP and KOL engagement, ensuring adherence to regulatory guidelines (e.g., FDA, ICH).</li>\n<li>Create and refine the clinical scientific and value story for deramiocel through internal consultations, external expert input, and data analysis to support program progression.</li>\n<li>Lead scientific communications, including publications, congress presentations, and medical information responses, while overseeing vendors as needed.</li>\n<li>Provide medical expertise to support commercialization readiness activities, including training, payer interactions, and real-world evidence initiatives.</li>\n<li>Work cross-functionally with clinical development, regulatory affairs, commercial, and quality teams to drive business impact and team success.</li>\n<li>Identify opportunities for continuous improvement in medical affairs operations, fostering a culture of innovation and compliance.</li>\n<li>Monitor emerging scientific data, competitive landscape, and therapeutic trends in neurology, myology, cardiology, and rare diseases to inform strategy.</li>\n<li>Perform such other duties as may be assigned from time to time.</li>\n"},{"text":"Requirements","content":"\n<li>MD required, with experience in neurology, myology, cardiology, or a closely related field, and demonstrated clinical scientific competence.</li>\n<li>Deep experience and commitment to excellence in medical affairs, with a proven track record in biotechnology or pharmaceuticals.</li>\n<li>Experience working in a small company environment, thriving in dynamic, resource-constrained settings.</li>\n<li>Passionate \"can-do\" mentality with evidence of high emotional intelligence (EQ) and collaborative teamwork.</li>\n<li>Exceptional communication, presentation, and interpersonal skills to engage stakeholders at all levels.</li>\n<li>Strong understanding of regulatory compliance, including cGMP, ICH, and FDA guidelines.</li>\n<li>Ability to work independently, multi-task, and meet aggressive deadlines in a fast-paced environment.</li>\n<li>Willingness to travel up to 30-40% for meetings, site visits, and conferences.</li>\n"},{"text":"Preferred Qualifications","content":"\n<li>Previous experience with DMD, BMD, or other muscle or cardiomyopathic indications.</li>\n<li>Experience with pre-launch or commercialization activities in a Medical Affairs capacity.</li>\n<li>Experience with complex cell or gene therapy (ATMP) products.</li>\n"},{"text":"Work Environment and Physical Demands","content":"\n<li>Professional office (San Diego) or remote work environment.</li>\n<li>Prolonged periods of computer use for planning, documentation, and reporting.</li>\n<li>Occasional travel may be required for meetings, site visits, and stakeholder engagement.</li>\n<li>Ability to lift office materials up to 20 pounds.</li>\n"}],"salaryRange":{"max":350000,"currency":"USD","interval":"per-year-salary","min":300000},"text":"Senior Director, Medical Affairs (MD Required)","country":"US","workplaceType":"remote","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>Capricor is seeking Senior Director of Medical Affairs with deep expertise in biotechnology, ideally in rare diseases or cell therapies. This position will play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. This individual will define the roadmap for our scientific narrative, drive clinical scientific messaging, foster key relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), and patient advocacy groups in the DMD and BMD communities, and ensure high-integrity, compliant processes for stakeholder engagement. This new headcount position supports our major milestone of positive Phase 3 results and continued advancement of deramiocel. They will lead cross-functional efforts to bridge clinical development with commercialization readiness, fostering deep relationships and evidence generation strategies necessary to drive program success and ongoing medical excellence.</div>","descriptionBodyPlain":"Capricor is seeking Senior Director of Medical Affairs with deep expertise in biotechnology, ideally in rare diseases or cell therapies. This position will play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. This individual will define the roadmap for our scientific narrative, drive clinical scientific messaging, foster key relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), and patient advocacy groups in the DMD and BMD communities, and ensure high-integrity, compliant processes for stakeholder engagement. This new headcount position supports our major milestone of positive Phase 3 results and continued advancement of deramiocel. They will lead cross-functional efforts to bridge clinical development with commercialization readiness, fostering deep relationships and evidence generation strategies necessary to drive program success and ongoing medical excellence.\n","hostedUrl":"https://jobs.lever.co/capricor/079eb323-62ae-415b-9d52-fac80496067a","applyUrl":"https://jobs.lever.co/capricor/079eb323-62ae-415b-9d52-fac80496067a/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Assurance","allLocations":["San Diego, CA"]},"createdAt":1777475630625,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Senior Director of Quality provides strategic and operational leadership for all quality activities supporting Capricor’s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX™-based programs.\n \nThe Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>The Senior Director of Quality provides strategic and operational leadership for all quality activities supporting Capricor’s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX™-based programs.</div>\n<div>&nbsp;</div>\n<div>The Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.</div>","id":"1bf57252-056b-4d55-b8ed-3574b7230721","lists":[{"text":"Responsibilities","content":"<div>\n<p data-start=\"129\" data-end=\"340\">The Senior Director, Quality will provide strategic vision and operational direction for the Quality organization to ensure all programs meet the highest standards of safety, efficacy, and regulatory compliance.</p>\n</div>\n<div>&nbsp;</div>\n<div><strong>Quality Strategy &amp; Leadership</strong></div>\n\n<li>Define and execute the enterprise quality strategy aligned with late-stage clinical development, BLA/regulatory submissions, potential commercial launch, and post-approval lifecycle management for cell and exosome-based therapies.</li>\n<li>Serve as the senior Quality leader and strategic advisor to executive and operations management on compliance matters, inspection readiness, quality risk management, and GxP expectations in a biotech environment.</li>\n<li>Establish and reinforce a strong quality culture emphasizing accountability, data integrity, continuous improvement, and risk-based decision-making throughout the organization.</li>\n\n<div>&nbsp;</div>\n<div><strong>Enterprise Quality Systems</strong></div>\n\n<li>Own and continuously enhance the enterprise QMS to support clinical, manufacturing, and commercial operations, including Document Control and Change Management, Deviations/Investigations/CAPA, Training and Qualification, Data Integrity and Records Management, and other core quality processes.</li>\n<li>Ensure quality systems are phase-appropriate, scalable, efficient, and fully aligned with FDA GMP regulations (21 CFR Parts 210/211, 820, and biologics-specific guidance), ICH guidelines, ISO standards, and global expectations for advanced therapies.</li>\n<li>Lead QMS readiness and optimization for commercialization, pre-approval inspections (PAIs), post-approval commitments, and lifecycle management of Deramiocel and future products.</li>\n\n<div>&nbsp;</div>\n<div><strong>Regulatory Compliance &amp; Inspection Readiness</strong></div>\n\n<li>Ensure ongoing compliance with FDA, GMP, and applicable global regulations for clinical trials, manufacturing, and potential commercial activities, including cell therapy and exosome platforms.</li>\n<li>Lead preparation for, management of, and response to regulatory inspections (including PAIs), partner audits, and health authority interactions; act as the primary Quality representative during agency engagements and inspections.</li>\n<li>Support quality-related aspects of regulatory submissions, responses to information requests, and commitments (e.g., contributing to BLA updates addressing any quality/CMC items).</li>\n\n<div>&nbsp;</div>\n<div><strong>Clinical, Manufacturing &amp; Commercial Quality Oversight</strong></div>\n\n<li>Provide comprehensive quality oversight for clinical quality assurance, including GCP compliance and support for ongoing trials such as HOPE-3 extensions or related activities.</li>\n<li>Oversee quality support for manufacturing, testing, process validation, technology transfer, comparability studies, and supply chain activities for late-stage and commercial products (e.g., Deramiocel cell therapy production).</li>\n<li>Ensure timely and effective resolution of quality events, deviations, CAPAs, complaints, and out-of-specification results, with appropriate escalation, root cause analysis, and management visibility.</li>\n<li>Support commercial readiness activities, including product release processes, distribution oversight, post-market quality monitoring, and pharmacovigilance integration as applicable.</li>\n\n<div>&nbsp;</div>\n<div><strong>Cross-Functional Partnership</strong></div>\n\n<li>Collaborate closely with Clinical, Regulatory Affairs, CMC/Process Development, Manufacturing, Supply Chain, Quality Control, and Commercial teams to integrate quality principles throughout the product lifecycle and enable efficient, compliant decision-making.</li>\n<li>Provide risk-based quality guidance to support regulatory submissions, responses, and commitments while balancing compliance with operational agility in a fast-paced biotech setting.</li>\n\n<div>&nbsp;</div>\n<div><strong>Quality Metrics &amp; Continuous Improvement</strong></div>\n\n<li>Establish, monitor, and report quality KPIs, trends, risk indicators, and compliance metrics to senior leadership and the Quality Management Review.</li>\n<li>Drive continuous improvement initiatives, including process optimizations, lessons learned from inspections/audits, and enhancements to strengthen compliance maturity, operational efficiency, and inspection outcomes.</li>\n<li>Use data analytics and trending to proactively identify, assess, and mitigate quality risks across the portfolio.</li>\n\n<div>&nbsp;</div>\n<div><strong>People Leadership</strong></div>\n\n<li>Build, lead, and mentor a high-performing QA and Quality Systems organization; develop talent, succession plans, and training programs to support organizational scaling and commercialization milestones.</li>\n<li>Foster a collaborative, accountable, and inspection-ready mindset across the quality team and broader company.</li>\n"},{"text":"Requirements","content":"\n<li>Bachelor’s degree in Life Sciences, Engineering, Pharmacy, or a related field; advanced degree (e.g., MS, PhD) preferred.</li>\n<li>12+ years of progressive Quality Assurance experience in pharmaceutical or biotechnology environments, with significant focus on biologics, cell therapies, or advanced therapy medicinal products.</li>\n<li>7+ years of senior leadership experience with direct ownership and oversight of enterprise Quality Management Systems in a growing organization.</li>\n<li>Hands-on experience supporting late-stage clinical programs, BLA submissions, pre-approval inspections (PAIs), and commercial readiness/launch activities for regenerative medicine or biologics products.</li>\n<li>Deep knowledge of FDA regulations (including 21 CFR Parts 210/211, 820, biologics-specific guidance), GMP, ICH guidelines (Q8-Q12, etc.), and global standards relevant to cell and exosome therapies.</li>\n<li>Demonstrated success leading regulatory inspections (PAIs, routine GMP inspections), responding to findings, and maintaining inspection readiness in dynamic settings.</li>\n<li>Proven ability to scale QMS and quality organizations in a rapidly growing biotech company preparing for commercialization.</li>\n<li>Strong executive presence with the ability to influence, collaborate with, and advise cross-functional teams and senior leadership.</li>\n<li>Excellent communication, problem-solving, decision-making, and strategic thinking skills.</li>\n"},{"text":"Work Environment / Physical Demands","content":"\n<li>Office-based with routine presence in GMP manufacturing and laboratory environments to support oversight, audits, inspections, and quality activities.</li>\n<li>Extended periods of computer use for documentation review, data analysis, metrics reporting, and quality system management.</li>\n<li>Occasional lifting of office or light materials up to 10 pounds.</li>\n<li>Ability to navigate office, laboratory, and GMP manufacturing settings, with occasional travel for inspections, audits, or regulatory meetings as needed.</li>\n"}],"salaryRange":{"min":210000,"max":260000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Director, Quality","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>The Senior Director of Quality provides strategic and operational leadership for all quality activities supporting Capricor&rsquo;s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX&trade;-based programs.</div>\n<div>&nbsp;</div>\n<div>The Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.</div>","descriptionBodyPlain":"The Senior Director of Quality provides strategic and operational leadership for all quality activities supporting Capricor’s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX™-based programs.\n \nThe Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.\n","hostedUrl":"https://jobs.lever.co/capricor/1bf57252-056b-4d55-b8ed-3574b7230721","applyUrl":"https://jobs.lever.co/capricor/1bf57252-056b-4d55-b8ed-3574b7230721/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"IT","allLocations":["San Diego, CA"]},"createdAt":1775696526322,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nWe are seeking a highly skilled and hands-on Senior Systems Engineer to design, implement, and support enterprise IT infrastructure in a fast-paced biotech environment. This role will be responsible for maintaining highly available, secure, and scalable systems across cloud and on-prem environments.\nThe ideal candidate brings deep expertise in systems engineering, cloud platforms, automation, and security, with experience operating in regulated environments (GMP, SOX, etc.).\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<p>We are seeking a highly skilled and hands-on Senior Systems Engineer to design, implement, and support enterprise IT infrastructure in a fast-paced biotech environment. This role will be responsible for maintaining highly available, secure, and scalable systems across cloud and on-prem environments.</p>\n<p>The ideal candidate brings deep expertise in systems engineering, cloud platforms, automation, and security, with experience operating in regulated environments (GMP, SOX, etc.).</p>\n</div>","id":"54114b7b-8a41-4828-94aa-8a700323bd33","lists":[{"text":"Key Responsibilities ","content":"<div>\n<p><strong>Systems Engineering &amp; Infrastructure</strong></p>\n<ul type=\"disc\">\n<li>Design, implement, and maintain enterprise infrastructure (Windows/Linux servers, virtualization, storage)</li>\n<li>Manage hybrid environments spanning on-prem and cloud (AWS/Azure)</li>\n<li>Ensure high availability, performance, and scalability of systems</li>\n<li>Lead infrastructure upgrades, patching, and lifecycle management</li>\n\n<div align=\"center\"><hr width=\"100%\" size=\"2\" align=\"center\"></div>\n<p><strong>Cloud &amp; Modernization</strong></p>\n<ul type=\"disc\">\n<li>Architect and support cloud infrastructure in AWS and/or Azure</li>\n<li>Lead cloud migrations and optimization initiatives</li>\n<li>Optimize cost, performance, and reliability of cloud resources</li>\n\n<div align=\"center\"><hr width=\"100%\" size=\"2\" align=\"center\"></div>\n<p><strong>Security &amp; Compliance</strong></p>\n<ul type=\"disc\">\n<li>Implement and maintain system security best practices</li>\n<li>Partner with security teams on vulnerability management and remediation</li>\n<li>Ensure compliance with GMP, SOX, and FDA requirements</li>\n<li>Manage identity and access controls (SSO, MFA, RBAC)</li>\n\n<div align=\"center\"><hr width=\"100%\" size=\"2\" align=\"center\"></div>\n<p><strong>Monitoring, Automation &amp; Performance</strong></p>\n<ul type=\"disc\">\n<li>Implement and maintain monitoring and alerting solutions</li>\n<li>Automate repetitive tasks using scripting (PowerShell)</li>\n<li>Perform root cause analysis and performance tuning</li>\n<li>Maintain system documentation</li>\n\n<div align=\"center\"><hr width=\"100%\" size=\"2\" align=\"center\"></div>\n<p><strong>Collaboration &amp; Escalation Support</strong></p>\n<ul type=\"disc\">\n<li>Act as Tier 3 escalation point for complex infrastructure issues</li>\n<li>Partner with Help Desk, Network, and Security teams</li>\n<li>Support IT projects and cross-functional initiatives</li>\n<li>Provide technical mentorship to junior engineers</li>\n\n</ul></ul></ul></ul></ul></div>"},{"text":"Minimum Qualifications","content":"<div>\n<ul type=\"disc\">\n<li>Bachelor’s degree in IT, Computer Science, or related field (or equivalent experience)</li>\n<li>6+ years of experience in systems engineering or infrastructure roles</li>\n<li>Strong expertise in: Windows Server &amp; Active Directory, Linux systems administration, Virtualization (VMware, Hyper-V), Cloud platforms (AWS and/or Azure), Backup solutions (VEEAM)</li>\n<li>Experience with scripting/automation (PowerShell)</li>\n<li>Experience with backup, disaster recovery, and high availability design</li>\n\n</ul></div>"},{"text":"Preferred Qualifications","content":"<div>\n<ul type=\"disc\">\n<li>Experience in biotech, pharma, or regulated environments</li>\n<li>Knowledge of GMP, HIPAA, SOX, or FDA compliance frameworks</li>\n<li>Certifications such as: Microsoft (Azure Administrator/Architect), AWS Solutions Architect, and VMware (VCP)</li>\n<li>Experience with enterprise tools such as: Microsoft Intune, SolarWinds, Palo Alto Networks, and Veeam backup solution</li>\n\n</ul></div>"},{"text":"Key Competencies","content":"<div>\n<ul type=\"disc\">\n<li>Strong troubleshooting and root cause analysis skills</li>\n<li>Ability to work independently and manage complex systems</li>\n<li>Excellent documentation and organizational skills</li>\n<li>Strong communication with both technical and non-technical stakeholders</li>\n<li>Proactive, automation-first mindset</li>\n\n</ul></div>"}],"salaryRange":{"min":140000,"max":160000,"currency":"USD","interval":"per-year-salary"},"text":"Senior Systems Engineer","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<p>We are seeking a highly skilled and hands-on Senior Systems Engineer to design, implement, and support enterprise IT infrastructure in a fast-paced biotech environment. This role will be responsible for maintaining highly available, secure, and scalable systems across cloud and on-prem environments.</p>\n<p>The ideal candidate brings deep expertise in systems engineering, cloud platforms, automation, and security, with experience operating in regulated environments (GMP, SOX, etc.).</p>\n</div>","descriptionBodyPlain":"We are seeking a highly skilled and hands-on Senior Systems Engineer to design, implement, and support enterprise IT infrastructure in a fast-paced biotech environment. This role will be responsible for maintaining highly available, secure, and scalable systems across cloud and on-prem environments.\nThe ideal candidate brings deep expertise in systems engineering, cloud platforms, automation, and security, with experience operating in regulated environments (GMP, SOX, etc.).\n","hostedUrl":"https://jobs.lever.co/capricor/54114b7b-8a41-4828-94aa-8a700323bd33","applyUrl":"https://jobs.lever.co/capricor/54114b7b-8a41-4828-94aa-8a700323bd33/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego - SD3","team":"Quality Compliance","allLocations":["San Diego - SD3"]},"createdAt":1779410188648,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThe Supplier Quality Specialist/Supervisor is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. Reporting to Senior Manager Quality Compliance, this position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor’s commitment to quality and excellence in the development of innovative therapies. \nThe team this person will be joining develops and maintains the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs. \n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<div>\n<p><span data-contrast=\"auto\">The Supplier Quality Specialist/Supervisor is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. Reporting to Senior Manager Quality Compliance, this position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor’s commitment to quality and excellence in the development of innovative therapies.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">The team this person will be joining develops and&nbsp;maintains&nbsp;the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>","id":"d31b3656-b9ca-4b50-bab6-30a6fdd926dd","lists":[{"text":"Responsibilities ","content":"<div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Develop and Maintain Supplier Quality Program: Create, implement, and sustain a comprehensive supplier quality program to ensure consistent quality across the supply chain.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Manage Audit Programs:&nbsp;Establish&nbsp;and oversee Capricor’s external audit programs to ensure compliance with regulatory standards.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Create Supplier Scorecards: Develop and&nbsp;maintain&nbsp;scorecards to evaluate supplier performance and drive accountability.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ensure Audit Readiness:&nbsp;Maintain&nbsp;audit readiness and compliance with GMP and other regulatory standards.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Conduct Supplier Qualifications and Audits: Perform supplier qualifications and risk-based audits to ensure supplier compliance and quality.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"6\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Manage SCAR Activities: Oversee all supplier corrective action request (SCAR) processes, ensuring&nbsp;timely&nbsp;resolution of issues.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Generation and Management of Quality Agreements: Author, negotiate, and&nbsp;maintain&nbsp;Supplier Quality Agreements to clearly define roles, responsibilities, and quality expectations.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"8\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Collaborate on Material Specifications: Work with cross-departmental teams to develop and refine material specifications.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"9\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Prepare Quality Metrics: Compile and present quality metrics to stakeholders to support decision-making.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"10\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Address Quality Issues: Partner with internal teams to resolve supplier quality and audit-related challenges.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"11\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Drive Best Practices: Contribute to the development and implementation of best practices to enhance compliance and performance.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"12\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Perform Data Analysis: Conduct data analysis and&nbsp;maintain&nbsp;organized records, reports, and databases to support quality processes.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"13\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Implement Continuous Improvement: Recommend and implement measures to enhance quality processes and operational efficiency.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"14\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Train Employees: Provide training on relevant quality procedures to ensure consistent adherence across teams.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"15\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Develop SOPs: Write or revise QA/QC/Supply Chain Standard Operating Procedures (SOPs) to&nbsp;maintain&nbsp;compliance.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"16\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Present Data Internally: Deliver data-driven insights to support decision-making and quality initiatives.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"17\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Work Independently:&nbsp;Operate&nbsp;with minimal supervision to achieve project goals and meet deadlines.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"18\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Review and Approve Documents: Review and approve assigned documents to ensure accuracy and compliance.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"7\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"19\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Perform Additional Duties: Undertake other quality-related responsibilities as assigned to support organizational&nbsp;objectives.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"},{"text":"Requirements ","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Bachelor’s degree in a relevant Biological Science discipline required.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">7+ years of experience in a GMP Quality Control laboratory or GMP/GLP setting required, with direct experience in Supplier Quality Management and corporate/supplier audits.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Proven experience conducting audits as a lead auditor, ensuring compliance with internal and external quality standards.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">7+ years of hands-on experience in qualifying suppliers and vendors, including risk assessments, capability evaluations, and ongoing performance monitoring.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">SCAR Management: Extensive experience managing Supplier Corrective Action Requests (SCARs), from initiation through closure, ensuring&nbsp;timely&nbsp;and effective resolution of quality issues.</span></p>\n</li>\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">&nbsp;Skilled in drafting, revising, and maintaining SOPs to support quality system effectiveness and regulatory compliance.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"7\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Supplier Quality Agreements:&nbsp;Demonstrated&nbsp;expertise&nbsp;in authoring, negotiating, and&nbsp;maintaining&nbsp;Supplier Quality Agreements to clearly define roles, responsibilities, and quality expectations.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>"},{"text":"Preferred Qualification ","content":"<div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"8\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Proficiency in Outlook, MS Office, and other electronic systems; experience with aseptic processing a plus.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"9\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Excellent communication, time-management, and teamwork skills to collaborate effectively across departments.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"10\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Strong organizational skills and attention to detail to manage records, reports, and databases.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"11\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to prioritize and manage multiple responsibilities in a fast-paced environment.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"12\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">&nbsp;Ability to gown and work in classified areas for audits or inspections.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"13\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Ability to independently perform tasks, generate reports, and escalate issues as needed.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"14\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">ASQ CQA certification preferred; candidates without current certification must&nbsp;demonstrate&nbsp;a willingness and ability to obtain certification within a specified&nbsp;timeframe.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"8\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"15\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Strong team&nbsp;player with the ability to collaborate effectively across cross-functional departments.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n</div>\n</div>"},{"text":"Work Environment and Physical Demands ","content":"<div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Setting: Primarily office- and laboratory-based, focusing on supplier quality management, audits, and documentation, in an office or hybrid arrangement due to limited office space.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Physical Requirements: Requires gowning and working in classified areas; involves prolonged periods of computer use for data analysis, report generation, and SOP development; occasional lifting of office materials or equipment up to 20 pounds.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<ul role=\"list\" style=\"list-style-type: disc;\">\n<li aria-setsize=\"-1\" data-leveltext=\"\" data-font=\"Symbol\" data-listid=\"9\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\" role=\"listitem\">\n<p><span data-contrast=\"auto\">Travel: Occasional travel may be&nbsp;required&nbsp;for supplier audits or vendor meetings.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</li>\n\n</ul></div>\n<div>\n<p><span data-contrast=\"auto\">Why&nbsp;Capricor?</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">Capricor&nbsp;Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient-centered innovation. Join us and be part of a team&nbsp;that’s&nbsp;changing lives—help us&nbsp;shape&nbsp;the future of healthcare.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span data-contrast=\"auto\">This role offers the ability to develop and execute vendor programs that align with the organization's vision and growth&nbsp;objectives. You will develop partnerships where vendor insights,&nbsp;expertise, and strategic perspectives are recognized and valued.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>"}],"salaryRange":{"min":120000,"max":140000,"currency":"USD","interval":"per-year-salary"},"salaryDescription":"<div><span data-contrast=\"auto\">Comprehensive benefits package, including health insurance, retirement plans, equity awards, and opportunities for professional development.</span><span data-ccp-props=\"{}\">&nbsp;</span></div>","salaryDescriptionPlain":"Comprehensive benefits package, including health insurance, retirement plans, equity awards, and opportunities for professional development. \n","text":"Supplier Quality Management (SQM) Manager","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<div>\n<p><span xml:lang=\"EN-US\" data-contrast=\"auto\">The Supplier Quality Specialist/Supervisor is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. Reporting to Senior Manager Quality Compliance, this position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor&rsquo;s commitment to quality and excellence in the development of innovative therapies.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n<div>\n<p><span xml:lang=\"EN-US\" data-contrast=\"auto\">The team this person will be joining develops and&nbsp;maintains&nbsp;the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs.</span><span data-ccp-props=\"{}\">&nbsp;</span></p>\n</div>\n</div>","descriptionBodyPlain":"The Supplier Quality Specialist/Supervisor is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. Reporting to Senior Manager Quality Compliance, this position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor’s commitment to quality and excellence in the development of innovative therapies. \nThe team this person will be joining develops and maintains the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs. \n","hostedUrl":"https://jobs.lever.co/capricor/d31b3656-b9ca-4b50-bab6-30a6fdd926dd","applyUrl":"https://jobs.lever.co/capricor/d31b3656-b9ca-4b50-bab6-30a6fdd926dd/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Quality Engineering","allLocations":["San Diego, CA"]},"createdAt":1774540417946,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nWe are seeking an experienced Veeva Vault EQMS Specialist with deep expertise in Veeva Vault, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross‑functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future‑ready quality operations.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>We are seeking an experienced <strong>Veeva Vault EQMS Specialist</strong>&nbsp;with deep expertise in Veeva Vault, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross‑functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future‑ready quality operations.</div>","id":"67b32650-3fc5-49dd-badc-2b217b7b5f52","lists":[{"text":"Responsibilities:","content":"\n<li>Lead or support end-to-end implementation of <strong>Veeva Vault Quality Suite</strong>, including requirements gathering, configuration, testing, validation, and go-live activities.</li>\n<li>Translate business needs into functional specifications and system design within Veeva Vault.</li>\n<li>Configure and optimize workflows, document types, metadata, training assignments, quality processes, and user roles.</li>\n<li>Conduct detailed process mapping of current-state and future-state EQMS processes (e.g., Document Management, Change Control, Deviations, CAPA, Complaints, Training).</li>\n<li>Facilitate workshops with cross-functional stakeholders to define requirements and align system capabilities with business objectives.</li>\n<li>Identify opportunities for process improvements and automation within Veeva.</li>\n<li>Support or lead system validation activities including user requirements (URS), functional specifications, IQ/OQ/PQ, and change control in compliance with GxP and 21 CFR Part 11.</li>\n<li>Ensure adherence to internal quality standards, regulatory expectations, and IT/CSV methodologies.</li>\n<li><strong>Testing &amp; Deployment</strong></li>\n<li>Develop and execute test scripts, manage defects, and facilitate UAT sessions.</li>\n<li>Support go-live planning, cutover activities, and hypercare.</li>\n<li>Maintain updates to Veeva releases, including impact assessments and regression testing.</li>\n<li><strong>Training &amp; Support</strong></li>\n<li>Develop user training materials and deliver hands-on training for business end users.</li>\n<li>Provide ongoing support, troubleshoot issues, and manage enhancement requests.</li>\n<li>Serve as a subject matter expert (SME) for Veeva Vault within the Quality organization.</li>\n"},{"text":"Requirements:","content":"\n<li>3+ years of experience as a Business Analyst in Life Sciences Quality (Pharma, Biotech, or Medical Devices).</li>\n<li>\n<div>Hands-on experience with full Veeva Vault implementations, ideally within the Vault Quality Suite (QualityDocs, QMS, Training).</div>\n</li>\n<li>\n<div>Strong working knowledge of GxP, 21 CFR Part 11, Annex 11, and core quality system processes.</div>\n</li>\n<li>\n<div>Experience with computer system validation (CSV) and creation of validation documentation.</div>\n</li>\n<li>\n<div>Excellent communication skills with the ability to translate technical concepts for non-technical audiences.</div>\n</li>\n<li>\n<div>Strong analytical, problem‑solving, and stakeholder management capabilities.</div>\n</li>\n<li>Must be able to work <strong>on site</strong> Monday to Friday.</li>\n"},{"text":"Preferred Qualifications:","content":"\n<li>Veeva Vault Administrator or Vault Quality certification.</li>\n<li>Experience working with global teams and regulated environments.</li>\n<li>Familiarity with integration tools, APIs, and downstream/upstream system interfaces.</li>\n<li>Experience in managing enhancements post-implementation and supporting continuous improvement.</li>\n"}],"salaryRange":{"min":90000,"max":115000,"currency":"USD","interval":"per-year-salary"},"text":"Veeva Vault EQMS Specialist","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>We are seeking an experienced <strong>Veeva Vault EQMS Specialist</strong>&nbsp;with deep expertise in Veeva Vault, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross‑functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future‑ready quality operations.</div>","descriptionBodyPlain":"We are seeking an experienced Veeva Vault EQMS Specialist with deep expertise in Veeva Vault, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross‑functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future‑ready quality operations.\n","hostedUrl":"https://jobs.lever.co/capricor/67b32650-3fc5-49dd-badc-2b217b7b5f52","applyUrl":"https://jobs.lever.co/capricor/67b32650-3fc5-49dd-badc-2b217b7b5f52/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Warehouse Operations","allLocations":["San Diego, CA"]},"createdAt":1776097073228,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","id":"c45a15b1-dd28-4639-83cc-4193e68f1770","lists":[{"text":"Responsibilities","content":"<div>\n\n<li>Performs all duties of Material Handler III</li>\n<li>Oversee daily warehouse activities, including receiving, storing, and distributing materials and products.</li>\n<li>Receives all GMP items on an electronic inventory system - verify count, vendor item,&nbsp;number, and expiration date against item specification and purchase order before&nbsp;printing the bar code label.</li>\n<li>Maintain accurate inventory records, conduct regular audits, and ensure proper stock&nbsp;levels.</li>\n<li>Lead and mentor a team of warehouse staff, providing training and support to ensure&nbsp;high performance and adherence to safety protocols.</li>\n<li>Ensure that all products are stored and handled according to company standards and&nbsp;regulatory requirements.</li>\n<li>Ensure compliance with safety regulations and company policies. Promote a culture of&nbsp;safety awareness among warehouse staff.</li>\n<li>Support Implementation and enforce safety procedures to maintain a safe working&nbsp;environment.</li>\n<li>Perform physical inventory management to ensure continuous production of drug&nbsp;products</li>\n<li>Coordinate with other departments to ensure timely and accurate delivery of&nbsp;materials and products.</li>\n<li>Assists in the writing and/or developing of Standard Operating Procedure (SOP)</li>\n<li>Support completing deviations and investigations regarding non-conforming products.</li>\n<li>Work with the electronic and paper-based inventory system to manage the receipt,&nbsp;release, packaging, and shipment of GMP materials</li>\n<li>Perform disposition of all expired materials and maintain applicable documentation.</li>\n<li>Monitor temperature conditions of refrigerators, freezers, and room temperature&nbsp;storage of cGMP materials, including responding to alarms (on-call), as necessary</li>\n<li>Identify opportunities for process improvement in warehouse operations.</li>\n<li>Maintain partnerships in job function and with assembly, materials, and logistics,&nbsp;across the manufacturing operations and across all shifts.</li>\n<li>Fills material requests and deliveries to manufacturing as required.</li>\n<li>Perform cycle audits and physical inventory per schedule.</li>\n<li>Help reconcile inventory discrepancies and report discrepancies to the Supervisor.</li>\n<li>Source and maintain necessary quality documents for the release of critical material.</li>\n<li>Maintain a library of material specs, forms, and other materials documents</li>\n<li>Flexible schedule and able to support all operational requirements</li>\n<li>Perform other duties as assigned to support Supply Chain</li>\n\n</div>"},{"text":"Minimum Qualifications ","content":"<div>\n\n<li>High school diploma or equivalent</li>\n<li>2+ years related experience in a GMP regulated warehouse / materials management</li>\n<li>2+ Experience with Inventory Management Systems/ERP environment in a biotech or life sciences environment</li>\n<li>Proven experience in warehouse supervision or lead roles, and inventory control,&nbsp;preferably in a manufacturing or distribution environment.</li>\n<li>Strong knowledge of warehouse operations, inventory management, and logistics&nbsp;principles.</li>\n<li>Proficiency in using warehouse management systems (WMS) and other relevant&nbsp;software.</li>\n<li>Effective leadership and communication skills. Ability to motivate and coach a diverse&nbsp;team.</li>\n<li>Ability to lift up 50lbs</li>\n\n</div>"},{"text":"Preferred Qualifications ","content":"\n<li>Associate's degree</li>\n<li>Attention to detail and ability to prioritize tasks in a fast-paced environment.</li>\n<li>Able to adjust to workload in a fast-paced environment</li>\n<li>Able to work independently with little or no supervision of day-to-day tasks</li>\n<li>Proficient in Microsoft Office applications such as Excel, Outlook, Word, PowerPoint</li>\n"}],"salaryRange":{"min":75000,"max":90000,"currency":"USD","interval":"per-year-salary"},"text":"Warehouse Lead","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/capricor/c45a15b1-dd28-4639-83cc-4193e68f1770","applyUrl":"https://jobs.lever.co/capricor/c45a15b1-dd28-4639-83cc-4193e68f1770/apply"},{"additionalPlain":"Why Capricor?\nCapricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.\n\nCome Work With Us!\nAt Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.\n\nPlease note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.\n\n\n\nNotice to Recruiting Agencies \nCapricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.\n","additional":"<div><b>Why Capricor?</b></div><div>Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.</div><div><br></div><div><b>Come Work With Us!</b></div><div>At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.</div><div><br></div><div><i>Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.</i></div><div><br></div><div><br></div><div><br></div><div><b>Notice to Recruiting Agencies </b></div><div>Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.</div>","categories":{"commitment":"Full-time (exempt)","department":"Capricor Therapeutics","location":"San Diego, CA","team":"Warehouse Operations","allLocations":["San Diego, CA"]},"createdAt":1776096301645,"descriptionPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n\n\nThis Warehouse Supervisor oversees daily incoming, inventory and replenishment operations to ensure timely receipts, accurate inventory management, organization and on time fulfillment to support all end users.\nThis Role will manage a team of materials handlers, leads to ensure adherence to company SOPs and all requirements with safety alignment. This role will support KPIs, Projects, SOP review, updates, and process improvements through change controls with collaborative partners and effectively using ERP.\n","description":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div><div><br></div><div>\n<p>This Warehouse Supervisor oversees daily incoming, inventory and replenishment operations&nbsp;to ensure timely receipts, accurate inventory management, organization and on time&nbsp;fulfillment to support all end users.</p>\n<p>This Role will manage a team of materials handlers, leads to ensure adherence to company&nbsp;SOPs and all requirements with safety alignment.&nbsp;This role will support KPIs, Projects, SOP review, updates, and process improvements through&nbsp;change controls with collaborative partners and effectively using ERP.</p>\n</div>","id":"b933f7b0-0f66-4ebc-aa18-6fc9fdc0761b","lists":[{"text":"Responsibilities","content":"<div>\n\n<li>Supervise and lead materials team, provide training, guidance and performance feedback.</li>\n<li>Plan schedule activities to meet operational requirements</li>\n<li>Oversee manage receipts, inventory accuracy and all replenishment need following FEF&nbsp;and ensuring traceability with ERP and associating documentation.</li>\n<li>Initiates and complete Investigations, corrective and preventive actions</li>\n<li>Initiates and complete Change Controls support implementations</li>\n<li>SOP and Work instructions updates and creation</li>\n<li>Reviews metrics and leads process improvements projects</li>\n<li>Ensure training and all requirements to support teams' performance are being coordinate,&nbsp;improved with quality and reviewed</li>\n<li>Able to support multiple warehouses and be onsite including traveling between sites as&nbsp;needed</li>\n<li>Flexible with shifts and hours required to support the business (e.i first shift, staggered&nbsp;shift and future changes to support development and expansion projects)</li>\n<li>Able to conduct meetings, utilizing Microsoft teams, prepare PowerPoints, Excel basic formulas effective communications throughout including outlook and collaborates well with&nbsp;all partners to drive results</li>\n<li>Support data for KPI’s for warehouse operations and improvements by gathering data.</li>\n<li>Proactively plan and have the ability to be reactive to support where needed.</li>\n<li>Perform all tasks assigned to support Supply Chain operations.</li>\n\n</div>"},{"text":"Requirements","content":"<div>\n\n<li>Minimum Associate’s degree/bachelor's degree preferred</li>\n<li>5+ years' experience of warehouse experience preferred</li>\n<li>5+ years of experience of ERP usage and Document management systems</li>\n<li>2 + years of supervision or 4+ years lead roles in GMP-regulated environments with&nbsp;progressive development and accomplishments.</li>\n<li>Equivalent combination of experience considered</li>\n<li>Strong knowledge of warehouse operations and quality expectations managing temperature sensitive products.</li>\n<li>2+ years of forklift, box trucks and all associating warehouse equipment including&nbsp;standalone cold/frozen storage units</li>\n<li>2-4 + years of supply chain and logistics</li>\n<li>DOT 49CFR, IATA understand and or certification preferred</li>\n<li>Excellent organization, leadership, and communication skills.</li>\n<li>Ability to lift up to 50 lbs and work in a fast-paced environment</li>\n\n</div>"},{"text":"Working Conditions ","content":"<div>\n\n<li>Office and warehouse environment.</li>\n<li>Flexible for operational requirements</li>\n\n</div>"}],"salaryRange":{"min":100000,"max":120000,"currency":"USD","interval":"per-year-salary"},"text":"Warehouse Supervisor","country":"US","workplaceType":"onsite","opening":"<div>Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.</div>","openingPlain":"Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.\n","descriptionBody":"<div>\n<p>This Warehouse Supervisor oversees daily incoming, inventory and replenishment operations&nbsp;to ensure timely receipts, accurate inventory management, organization and on time&nbsp;fulfillment to support all end users.</p>\n<p>This Role will manage a team of materials handlers, leads to ensure adherence to company&nbsp;SOPs and all requirements with safety alignment.&nbsp;This role will support KPIs, Projects, SOP review, updates, and process improvements through&nbsp;change controls with collaborative partners and effectively using ERP.</p>\n</div>","descriptionBodyPlain":"This Warehouse Supervisor oversees daily incoming, inventory and replenishment operations to ensure timely receipts, accurate inventory management, organization and on time fulfillment to support all end users.\nThis Role will manage a team of materials handlers, leads to ensure adherence to company SOPs and all requirements with safety alignment. This role will support KPIs, Projects, SOP review, updates, and process improvements through change controls with collaborative partners and effectively using ERP.\n","hostedUrl":"https://jobs.lever.co/capricor/b933f7b0-0f66-4ebc-aa18-6fc9fdc0761b","applyUrl":"https://jobs.lever.co/capricor/b933f7b0-0f66-4ebc-aa18-6fc9fdc0761b/apply"}]