[{"additionalPlain":"Landmark Bio is a Watertown, Massachusetts–based company focused on advancing the development and manufacturing of genetic medicines and other advanced therapies. The organization provides CMC development and GMP manufacturing capabilities for cell and gene therapies and works with industry partners to develop scalable manufacturing approaches that help bring new therapies to patients.\n\nLandmark Bio is an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply.\n\n","additional":"Landmark Bio is a Watertown, Massachusetts–based company focused on advancing the development and manufacturing of genetic medicines and other advanced therapies. The organization provides CMC development and GMP manufacturing capabilities for cell and gene therapies and works with industry partners to develop scalable manufacturing approaches that help bring new therapies to patients.
Landmark Bio is an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply.
","categories":{"commitment":"Full Time","department":"Business Development","location":"Northeast States","team":"Business Development","allLocations":["Northeast States"]},"createdAt":1770243873395,"descriptionPlain":"We are seeking a high-performing Director, Business Development, Eastern U.S., to join our growing commercial team, focused on building and expanding strategic relationships in the Cell and Gene Therapy (CGT) space. The ideal candidate is a proven hunter who thrives on identifying and developing new business, understands the complex needs of biopharma clients, and can confidently represent technical capabilities across multiple advanced therapy modalities.\nAs part of a cutting-edge CDMO organization, you will be responsible for driving revenue growth and expanding our footprint with biotech and pharma partners across the U.S.\n\nKey Responsibilities\n· Prospect, identify, and close new business opportunities within the CGT ecosystem, including biotech, pharma, and emerging therapeutics companies\n· Generate new business by actively engaging with potential clients, qualifying them, and ultimately converting them into paying clients \n· Develop and manage a territory plan focused on early stage to commercial partnerships\n· Effectively communicate technical capabilities in viral vector manufacturing, mRNA production, and cell & gene therapy platforms, with support from technical subject matter experts\n· Build strong, trust-based relationships with decision-makers across R&D, CMC, AP/PD, manufacturing and senior leadership teams\n· Drive the full sales cycle from lead generation through proposal development, negotiation, and close\n· Maintain accurate pipeline management and forecasting using CRM tools\n· Collaborate cross-functionally with marketing, technical teams, and program management to support client onboarding and long-term success\n· Consistently meet or exceed quarterly and annual forecast quotas\n\nQualifications\n· 5+ years of successful B2B sales experience, with a minimum of 2 years selling into the CGT/CDMO space\n· Strong understanding of viral vectors, mRNA, and/or cell & gene therapy platforms — deeper technical knowledge in at least one modality required\n· Bachelor’s degree in a scientific discipline required; Master’s or PhD preferred\n· Prior hands-on lab experience is highly valued and will support credibility with scientific buyers\n· Proven track record of consistently meeting or exceeding quota\n· Demonstrated ability to build and grow new accounts with minimal oversight\n· Highly self-motivated, strategic thinker, and comfortable navigating technical, multi-stakeholder sales cycles\n· Excellent verbal and written communication skills, with the ability to tailor messages to both scientific and business audiences\n- Ideally, candidate is located in the Northeast; other locations considered with strong qualifications\n","description":"We are seeking a high-performing Director, Business Development, Eastern U.S., to join our growing commercial team, focused on building and expanding strategic relationships in the Cell and Gene Therapy (CGT) space. The ideal candidate is a proven hunter who thrives on identifying and developing new business, understands the complex needs of biopharma clients, and can confidently represent technical capabilities across multiple advanced therapy modalities.
As part of a cutting-edge CDMO organization, you will be responsible for driving revenue growth and expanding our footprint with biotech and pharma partners across the U.S.
Key Responsibilities
· Prospect, identify, and close new business opportunities within the CGT ecosystem, including biotech, pharma, and emerging therapeutics companies
· Generate new business by actively engaging with potential clients, qualifying them, and ultimately converting them into paying clients
· Develop and manage a territory plan focused on early stage to commercial partnerships
· Effectively communicate technical capabilities in viral vector manufacturing, mRNA production, and cell & gene therapy platforms, with support from technical subject matter experts
· Build strong, trust-based relationships with decision-makers across R&D, CMC, AP/PD, manufacturing and senior leadership teams
· Drive the full sales cycle from lead generation through proposal development, negotiation, and close
· Maintain accurate pipeline management and forecasting using CRM tools
· Collaborate cross-functionally with marketing, technical teams, and program management to support client onboarding and long-term success
· Consistently meet or exceed quarterly and annual forecast quotas
Qualifications
· 5+ years of successful B2B sales experience, with a minimum of 2 years selling into the CGT/CDMO space
· Strong understanding of viral vectors, mRNA, and/or cell & gene therapy platforms — deeper technical knowledge in at least one modality required
· Bachelor’s degree in a scientific discipline required; Master’s or PhD preferred
· Prior hands-on lab experience is highly valued and will support credibility with scientific buyers
· Proven track record of consistently meeting or exceeding quota
· Demonstrated ability to build and grow new accounts with minimal oversight
· Highly self-motivated, strategic thinker, and comfortable navigating technical, multi-stakeholder sales cycles
· Excellent verbal and written communication skills, with the ability to tailor messages to both scientific and business audiences
- Ideally, candidate is located in the Northeast; other locations considered with strong qualifications
","id":"343af970-dc3a-4649-a71c-6c3c6d29cb85","lists":[],"text":"Director, Business Development - Eastern U.S.","country":"US","workplaceType":"remote","opening":"","openingPlain":"","descriptionBody":"We are seeking a high-performing Director, Business Development, Eastern U.S., to join our growing commercial team, focused on building and expanding strategic relationships in the Cell and Gene Therapy (CGT) space. The ideal candidate is a proven hunter who thrives on identifying and developing new business, understands the complex needs of biopharma clients, and can confidently represent technical capabilities across multiple advanced therapy modalities.
As part of a cutting-edge CDMO organization, you will be responsible for driving revenue growth and expanding our footprint with biotech and pharma partners across the U.S.
Key Responsibilities
· Prospect, identify, and close new business opportunities within the CGT ecosystem, including biotech, pharma, and emerging therapeutics companies
· Generate new business by actively engaging with potential clients, qualifying them, and ultimately converting them into paying clients
· Develop and manage a territory plan focused on early stage to commercial partnerships
· Effectively communicate technical capabilities in viral vector manufacturing, mRNA production, and cell & gene therapy platforms, with support from technical subject matter experts
· Build strong, trust-based relationships with decision-makers across R&D, CMC, AP/PD, manufacturing and senior leadership teams
· Drive the full sales cycle from lead generation through proposal development, negotiation, and close
· Maintain accurate pipeline management and forecasting using CRM tools
· Collaborate cross-functionally with marketing, technical teams, and program management to support client onboarding and long-term success
· Consistently meet or exceed quarterly and annual forecast quotas
Qualifications
· 5+ years of successful B2B sales experience, with a minimum of 2 years selling into the CGT/CDMO space
· Strong understanding of viral vectors, mRNA, and/or cell & gene therapy platforms — deeper technical knowledge in at least one modality required
· Bachelor’s degree in a scientific discipline required; Master’s or PhD preferred
· Prior hands-on lab experience is highly valued and will support credibility with scientific buyers
· Proven track record of consistently meeting or exceeding quota
· Demonstrated ability to build and grow new accounts with minimal oversight
· Highly self-motivated, strategic thinker, and comfortable navigating technical, multi-stakeholder sales cycles
· Excellent verbal and written communication skills, with the ability to tailor messages to both scientific and business audiences
- Ideally, candidate is located in the Northeast; other locations considered with strong qualifications
","descriptionBodyPlain":"We are seeking a high-performing Director, Business Development, Eastern U.S., to join our growing commercial team, focused on building and expanding strategic relationships in the Cell and Gene Therapy (CGT) space. The ideal candidate is a proven hunter who thrives on identifying and developing new business, understands the complex needs of biopharma clients, and can confidently represent technical capabilities across multiple advanced therapy modalities.\nAs part of a cutting-edge CDMO organization, you will be responsible for driving revenue growth and expanding our footprint with biotech and pharma partners across the U.S.\n\nKey Responsibilities\n· Prospect, identify, and close new business opportunities within the CGT ecosystem, including biotech, pharma, and emerging therapeutics companies\n· Generate new business by actively engaging with potential clients, qualifying them, and ultimately converting them into paying clients \n· Develop and manage a territory plan focused on early stage to commercial partnerships\n· Effectively communicate technical capabilities in viral vector manufacturing, mRNA production, and cell & gene therapy platforms, with support from technical subject matter experts\n· Build strong, trust-based relationships with decision-makers across R&D, CMC, AP/PD, manufacturing and senior leadership teams\n· Drive the full sales cycle from lead generation through proposal development, negotiation, and close\n· Maintain accurate pipeline management and forecasting using CRM tools\n· Collaborate cross-functionally with marketing, technical teams, and program management to support client onboarding and long-term success\n· Consistently meet or exceed quarterly and annual forecast quotas\n\nQualifications\n· 5+ years of successful B2B sales experience, with a minimum of 2 years selling into the CGT/CDMO space\n· Strong understanding of viral vectors, mRNA, and/or cell & gene therapy platforms — deeper technical knowledge in at least one modality required\n· Bachelor’s degree in a scientific discipline required; Master’s or PhD preferred\n· Prior hands-on lab experience is highly valued and will support credibility with scientific buyers\n· Proven track record of consistently meeting or exceeding quota\n· Demonstrated ability to build and grow new accounts with minimal oversight\n· Highly self-motivated, strategic thinker, and comfortable navigating technical, multi-stakeholder sales cycles\n· Excellent verbal and written communication skills, with the ability to tailor messages to both scientific and business audiences\n- Ideally, candidate is located in the Northeast; other locations considered with strong qualifications\n","hostedUrl":"https://jobs.lever.co/landmarkbio/343af970-dc3a-4649-a71c-6c3c6d29cb85","applyUrl":"https://jobs.lever.co/landmarkbio/343af970-dc3a-4649-a71c-6c3c6d29cb85/apply"},{"additionalPlain":"Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.\n","additional":"Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.
","categories":{"commitment":"Full Time","department":"Science and Technology Operations","location":"Watertown, MA","team":"Manufacturing","allLocations":["Watertown, MA"]},"createdAt":1778789096456,"descriptionPlain":"We are seeking a highly motivated, team-oriented individual with a strong desire to learn and grow in a manufacturing environment. As a Manufacturing Associate, you will support the production of clinical supply products under cGMP conditions. You will play an important role in ensuring safe, high-quality, and efficient manufacturing operations while developing foundational skills in a regulated environment.\n \nWorking as part of a cross-functional team, you will contribute to day-to-day manufacturing activities, support operational readiness, and help maintain compliance with quality and regulatory standards.\n","description":"We are seeking a highly motivated, team-oriented individual with a strong desire to learn and grow in a manufacturing environment. As a Manufacturing Associate, you will support the production of clinical supply products under cGMP conditions. You will play an important role in ensuring safe, high-quality, and efficient manufacturing operations while developing foundational skills in a regulated environment.
\n
\nWorking as part of a cross-functional team, you will contribute to day-to-day manufacturing activities, support operational readiness, and help maintain compliance with quality and regulatory standards.
","id":"cfb5d5c1-0c80-4e6f-b1ab-fd7735d8383b","lists":[{"text":"","content":"\n
Scope of Responsibilities:
\n
\n- Support manufacturing operations to produce clinical supply products under cGMP conditions in a Lean Manufacturing environment
\n- Execute routine production activities following batch records, standard operating procedures (SOPs), and work instructions
\n- Prepare, operate, and clean equipment and manufacturing areas in accordance with established procedures
\n- Accurately document manufacturing activities in compliance with GMP and company requirements
\n- Adhere to all safety guidelines, environmental health standards, and quality systems
\n- Assist with material handling activities, including staging, labeling, and inventory tracking
\n- Identify, document, and communicate deviations, non-conformances, or safety concerns
\n- Collaborate with cross-functional teams, including Quality Assurance and Manufacturing Sciences, to support production goals
\n- Participate in training programs to build technical expertise and maintain compliance qualifications
\n- Contribute to continuous improvement initiatives and support a culture of operational excellence
\n- Support manufacturing area readiness for production activities and inspections
\n\nQualifications:
\n\n- High school diploma or equivalent required; Associate’s or Bachelor’s degree in Science or Engineering preferred
\n- 0–2 years of experience in manufacturing, biotechnology, pharmaceutical operations, or a related field (internships or academic lab experience acceptable)
\n- Basic understanding of GMP and regulated environments preferred
\n- Strong attention to detail and ability to follow written and verbal instructions
\n- Effective communication and interpersonal skills
\n- Ability to work collaboratively in a team environment
\n- Willingness to learn and grow in a fast-paced, start-up environment
\n\nAdditional Requirements:
\n\n- Ability to work in a cleanroom environment and wear appropriate personal protective equipment (PPE)
\n- Flexibility to support shift-based operations, including evenings, weekends, or overtime as needed
\n\n
We are seeking a highly motivated, team-oriented individual with a strong desire to learn and grow in a manufacturing environment. As a Manufacturing Associate, you will support the production of clinical supply products under cGMP conditions. You will play an important role in ensuring safe, high-quality, and efficient manufacturing operations while developing foundational skills in a regulated environment.
\n
\nWorking as part of a cross-functional team, you will contribute to day-to-day manufacturing activities, support operational readiness, and help maintain compliance with quality and regulatory standards.
","descriptionBodyPlain":"We are seeking a highly motivated, team-oriented individual with a strong desire to learn and grow in a manufacturing environment. As a Manufacturing Associate, you will support the production of clinical supply products under cGMP conditions. You will play an important role in ensuring safe, high-quality, and efficient manufacturing operations while developing foundational skills in a regulated environment.\n \nWorking as part of a cross-functional team, you will contribute to day-to-day manufacturing activities, support operational readiness, and help maintain compliance with quality and regulatory standards.\n","hostedUrl":"https://jobs.lever.co/landmarkbio/cfb5d5c1-0c80-4e6f-b1ab-fd7735d8383b","applyUrl":"https://jobs.lever.co/landmarkbio/cfb5d5c1-0c80-4e6f-b1ab-fd7735d8383b/apply"},{"additionalPlain":"Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.\n","additional":"Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.
","categories":{"commitment":"Full Time","department":"Business Operations","location":"Watertown, MA","team":"Program Management","allLocations":["Watertown, MA"]},"createdAt":1779296616938,"descriptionPlain":"We are seeking a self-driven, team-oriented, and entrepreneurial-minded Senior Program Manager to join Landmark Bio. The Senior Program Manager has an in-depth understanding of the processes and systems required to manage complex programs and projects, including extensive experience with Smartsheet, along with a functional understanding of the technical aspects of cell and gene therapy programs and awareness of Landmark Bio’s business objectives.\nThe Senior Program Manager will support cross-functional program execution by driving operational coordination, maintaining program management tools and documentation, and serving as a key liaison between internal teams and external clients. This role is responsible for managing timelines, dashboards, communications, and process improvements while ensuring programs are executed efficiently and effectively.\n \n","description":"We are seeking a self-driven, team-oriented, and entrepreneurial-minded Senior Program Manager to join Landmark Bio. The Senior Program Manager has an in-depth understanding of the processes and systems required to manage complex programs and projects, including extensive experience with Smartsheet, along with a functional understanding of the technical aspects of cell and gene therapy programs and awareness of Landmark Bio’s business objectives.
\nThe Senior Program Manager will support cross-functional program execution by driving operational coordination, maintaining program management tools and documentation, and serving as a key liaison between internal teams and external clients. This role is responsible for managing timelines, dashboards, communications, and process improvements while ensuring programs are executed efficiently and effectively.
\n
","id":"13c6a8f3-28c2-4b49-b989-1a18c9db7cb3","lists":[{"text":"Responsibilities","content":"\n- Support the planning, coordination, and execution of internal and client-facing programs
\n- Develop and maintain program timelines, schedules, dashboards, and risk registers with support from senior program managers
\n- Coordinate program materials and shared resources, escalating constraints and risks as appropriate
\n- Generate and maintain documentation for program scope changes and client communications
\n- Assist with capturing and sharing lessons learned across programs to improve operational efficiency
\n- Create and update presentations for team meetings, leadership reviews, and client discussions
\n\n\n- Serve as a Smartsheet super user for the organization, creating, managing, and optimizing complex workflows, automations, dashboards, and reporting tools
\n- Develop and maintain program management resources including trackers, templates, dashboards, presentation materials, and other operational tools
\n- Evaluate and recommend process improvements to enhance team collaboration, visibility, and efficiency
\n- Collaborate cross-functionally on new system evaluations, tool implementations, and training initiatives
\n\n\n- Maintain internal Microsoft Teams sites and external SharePoint client sites to ensure documentation is organized, current, and accessible
\n- Archive program documentation at the close of programs in accordance with internal procedures
\n- Own and maintain program management documentation including:
\n\n- Program charters
\n- Program plans and schedules
\n- RACI matrices
\n- Risk registers
\n- Business requirements
\n- Policies and procedures
\n- Training materials
\n\n- Ensure all documentation is accurate, complete, version-controlled, and properly stored
\n\n\n- Serve as the primary point of contact for assigned clients
\n- Coordinate and manage client meetings, teleconferences, and onsite visits
\n- Prepare agendas, meeting minutes, action items, and follow-up communications
\n- Build collaborative relationships with internal stakeholders and external partners to support successful program delivery
\n- Assist in training personnel on evolving program management tools and systems
\n- Develop training materials including slide decks, guides, and reference documentation
\n
"},{"text":"Qualifications","content":"\nBS degree with 7+ years relevant experience (GMP pharmaceutical, biologics, and/or cell and gene therapy field) is required\nPMP certification desired\nHigh degree of proficiency in Smartsheet is required, including advanced skills in workflow design and implementation, template creation and management, user training and support, and reporting and analytics\nStrong communication, problem solving, planning, and project management skills\nAbility to support more than one project of a reasonable size simultaneously\n\n
"}],"salaryRange":{"currency":"USD","min":140000,"max":165000,"interval":"per-year-salary"},"text":"Senior Program Manager","country":"US","workplaceType":"hybrid","opening":"","openingPlain":"","descriptionBody":"We are seeking a self-driven, team-oriented, and entrepreneurial-minded Senior Program Manager to join Landmark Bio. The Senior Program Manager has an in-depth understanding of the processes and systems required to manage complex programs and projects, including extensive experience with Smartsheet, along with a functional understanding of the technical aspects of cell and gene therapy programs and awareness of Landmark Bio’s business objectives.
\nThe Senior Program Manager will support cross-functional program execution by driving operational coordination, maintaining program management tools and documentation, and serving as a key liaison between internal teams and external clients. This role is responsible for managing timelines, dashboards, communications, and process improvements while ensuring programs are executed efficiently and effectively.
\n
","descriptionBodyPlain":"We are seeking a self-driven, team-oriented, and entrepreneurial-minded Senior Program Manager to join Landmark Bio. The Senior Program Manager has an in-depth understanding of the processes and systems required to manage complex programs and projects, including extensive experience with Smartsheet, along with a functional understanding of the technical aspects of cell and gene therapy programs and awareness of Landmark Bio’s business objectives.\nThe Senior Program Manager will support cross-functional program execution by driving operational coordination, maintaining program management tools and documentation, and serving as a key liaison between internal teams and external clients. This role is responsible for managing timelines, dashboards, communications, and process improvements while ensuring programs are executed efficiently and effectively.\n \n","hostedUrl":"https://jobs.lever.co/landmarkbio/13c6a8f3-28c2-4b49-b989-1a18c9db7cb3","applyUrl":"https://jobs.lever.co/landmarkbio/13c6a8f3-28c2-4b49-b989-1a18c9db7cb3/apply"},{"additionalPlain":"","additional":"Landmark Bio is dedicated to translating cutting-edge research into life-changing therapies. The company provides CMC development and GMP manufacturing capabilities for cell and gene therapies and other novel modalities, and partners with academic, biotech, and industry collaborators to advance next-generation manufacturing technologies.
","categories":{"commitment":"Full Time","department":"Science and Technology Operations","location":"Watertown, MA","team":"Digital Integration & Data Sciences","allLocations":["Watertown, MA"]},"createdAt":1773331833972,"descriptionPlain":"","description":"\n
Landmark Bio is seeking an experienced, hands-on IT professional to oversee end-user technology, infrastructure, and IT operations supporting a regulated biotech environment. This role is responsible for maintaining reliable, secure, and scalable systems that support day-to-day business and laboratory operations.
\n
The Senior Manager, IT will lead IT operations, manage vendors and managed service providers, and partner with internal stakeholders to ensure technology solutions support business needs while maintaining compliance with regulatory and security requirements.
\n
This role requires strong technical depth, operational discipline, and the ability to work across multiple functions in a fast-moving organization.
\n
\n
1. IT Operations & Infrastructure
\n
\n- \n
Maintain and support on-premise and cloud-hosted infrastructure, end-user devices, networking, and business applications
\n \n- \n
Ensure high availability, performance, and security of IT systems
\n \n- \n
Support regulated GxP laboratory and manufacturing environments
\n \n- \n
Manage user accounts, access control, device provisioning, and software deployment
\n \n- \n
Oversee backup, disaster recovery, and monitoring systems
\n \n\nPlatforms include:
\n\n- \n
Microsoft 365, SharePoint, Teams, Office
\n \n- \n
Windows Server / Windows 10/11
\n \n- \n
Meraki network / Palo Alto firewall / VPN
\n \n- \n
FreshService, CyberReason, Kaseya, IT Glue, Autotask, Rocket Cyber, BullPhish, RMM, Spanning, Unitrends
\n \n- \n
Building security and monitoring systems
\n \n- \n
End-user hardware, printers, and conference room AV
\n \n- \n
Business systems including Smartsheet, Veeva, SAP, DocuSign, Okta, Adobe
\n \n- \n
Lab instrument user accounts and software installs
\n \n\n2. User Support & Experience
\n\n- \n
Ensure timely and effective IT support for employees and laboratory users
\n \n- \n
Improve reliability, usability, and performance of end-user systems
\n \n- \n
Partner with business teams to evaluate and implement new applications
\n \n- \n
Support onboarding, offboarding, and equipment lifecycle management
\n \n\n3. Vendor & Managed Service Provider Management
\n\n- \n
Coordinate with external IT vendors and service providers
\n \n- \n
Monitor performance, costs, and service quality
\n \n- \n
Assist with contract renewals, budgeting, and vendor selection
\n \n\n4. Compliance & Security
\n\n- \n
Maintain IT policies, procedures, and documentation
\n \n- \n
Support CSA / SDLC / GxP / audit readiness activities
\n \n- \n
Ensure systems meet cybersecurity and data protection standards
\n \n- \n
Support validation and regulated system controls where required
\n \n\n5. Projects & Continuous Improvement
\n\n- \n
Lead small to mid-size IT projects and system implementations
\n \n- \n
Identify opportunities to improve efficiency, automation, and reliability
\n \n- \n
Support site expansion, lab build-out, and new system deployments
\n \n\n
\n
\n- \n
Bachelor’s degree in Information Technology, Computer Science, or related field
\n \n- \n
8+ years of IT experience, preferably in biotech, pharma, or regulated industry
\n \n- \n
Strong hands-on experience with end-user systems, infrastructure, and networking
\n \n- \n
Experience supporting cloud, SaaS, and on-premise environments
\n \n- \n
Experience working in GxP / regulated / manufacturing / lab environments preferred
\n \n- \n
Experience managing vendors and managed service providers
\n \n- \n
Strong troubleshooting and problem-solving skills
\n \n- \n
Ability to work independently in a small, fast-paced organization
\n \n\n
\n
Landmark Bio is seeking an experienced, hands-on IT professional to oversee end-user technology, infrastructure, and IT operations supporting a regulated biotech environment. This role is responsible for maintaining reliable, secure, and scalable systems that support day-to-day business and laboratory operations.
\n
The Senior Manager, IT will lead IT operations, manage vendors and managed service providers, and partner with internal stakeholders to ensure technology solutions support business needs while maintaining compliance with regulatory and security requirements.
\n
This role requires strong technical depth, operational discipline, and the ability to work across multiple functions in a fast-moving organization.
\n