[{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
\n
Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
\n
 
\n
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
\n
 
\n
Benefits Summary:
\n
Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
\n
 
\n
The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
\n
","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Business Development","allLocations":["Bend, Oregon"]},"createdAt":1773445684831,"descriptionPlain":"The Account Manager, Commercial Manufacturing will drive the expansion of Serán’s commercial manufacturing portfolio for oral solid drug products by identifying, qualifying, and securing high‑value opportunities. The Account Manager will serve as the primary point of contact for prospective and existing clients, guiding them from initial engagement through term sheet negotiation, commercial supply agreement execution, and ongoing account management. This role will ensure each opportunity aligns with Serán’s technical capabilities, service offerings, and strategic growth objectives. Primary responsibilities will be to maintain strong client relationships throughout the commercial manufacturing lifecycle to support successful project execution and optimize utilization of Serán’s commercial manufacturing capacity.  \nThis role will join a highly skilled Business Development team that is strategically located throughout North America. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to company headquarters in Bend, Oregon and client sites as needed.  Preference will be given to those with international Business Development and Account Management experience for commercial manufacturing.  \n \n","description":"
The Account Manager, Commercial Manufacturing will drive the expansion of Serán’s commercial manufacturing portfolio for oral solid drug products by identifying, qualifying, and securing high‑value opportunities. The Account Manager will serve as the primary point of contact for prospective and existing clients, guiding them from initial engagement through term sheet negotiation, commercial supply agreement execution, and ongoing account management. This role will ensure each opportunity aligns with Serán’s technical capabilities, service offerings, and strategic growth objectives. Primary responsibilities will be to maintain strong client relationships throughout the commercial manufacturing lifecycle to support successful project execution and optimize utilization of Serán’s commercial manufacturing capacity.  
\n
\n

This role will join a highly skilled Business Development team that is strategically located throughout North America. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to company headquarters in Bend, Oregon and client sites as needed.  Preference will be given to those with international Business Development and Account Management experience for commercial manufacturing.  

\n
\n
 
","id":"b15bf1de-133a-4861-be34-5f3598641c28","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Identify, qualify, and pursue new commercial manufacturing opportunities for oral solid drug products
    • \n
  • Build and maintain a robust pipeline of prospects aligned with Serán’s technical capabilities and capacity strategy
    • \n
  • Conduct initial technical and commercial assessments to ensure strong project fit
    • \n
  • Lead the development and negotiation of term sheets and commercial supply agreements
    • \n
  • Serve as the primary point of contact for assigned commercial accounts, ensuring a high‑quality client experience
    • \n
  • Develop strong, trust‑based relationships with key stakeholders at client organizations
    • \n
  • Communicate project status, timelines, risks, and decisions clearly and proactively
    • \n
  • Support long‑term client retention and growth through strategic account planning
    • \n
  • Guide clients through the commercial manufacturing lifecycle—from onboarding and tech transfer through validation, launch, and ongoing supply
    • \n
  • Collaborate closely with internal teams (technical operations, quality, supply chain, finance, legal) to ensure smooth project execution
    • \n
  • Monitor project progress, identify risks or bottlenecks, and drive timely resolution
    • \n
  • Ensure commercial commitments, deliverables, and quality expectations are met
    • \n
  • Coordinate internal review and approval of commercial proposals, pricing, and contract terms
    • \n
  • Manage renewals, amendments, and long‑term supply agreements as client needs evolve
    • \n
  • Ensure accurate forecasting and demand planning to support capacity utilization
    • \n
  • Provide market insights and customer feedback to inform commercial strategy and capacity planning
    • \n
  • Maintain accurate CRM records, pipeline reporting, and revenue forecasting
    • \n
  • Contribute to continuous improvement of commercial processes, tools, and client engagement practices
    • \n
  • Support cross‑functional initiatives that enhance Serán’s commercial manufacturing capabilities and competitiveness
    • \n
  • Scope my increase to align with company initiatives
    • \n
  • Perform other related duties as assigned  
    • \n"},{"text":"Required Skills and Experience ","content":""},{"text":"Education and Experience ","content":"
    \n
    "},{"text":"Physical Requirement ","content":"
    \n\n
  • Prolonged periods of sitting at a desk and working on a computer
    • \n
  • Must be able to lift to 15 pounds at times
    • \n
  • Approximately 25% of travel required, and at times greater than 50%
    • \n
  • Travel will be predominately domestic with the potential for international travel
    • \n\n
    "}],"text":"Account Manager, Commercial Manufacturing","country":"US","workplaceType":"remote","opening":"","openingPlain":"","descriptionBody":"
    The Account Manager, Commercial Manufacturing will drive the expansion of Serán’s commercial manufacturing portfolio for oral solid drug products by identifying, qualifying, and securing high‑value opportunities. The Account Manager will serve as the primary point of contact for prospective and existing clients, guiding them from initial engagement through term sheet negotiation, commercial supply agreement execution, and ongoing account management. This role will ensure each opportunity aligns with Serán’s technical capabilities, service offerings, and strategic growth objectives. Primary responsibilities will be to maintain strong client relationships throughout the commercial manufacturing lifecycle to support successful project execution and optimize utilization of Serán’s commercial manufacturing capacity.  
    \n
    \n

    This role will join a highly skilled Business Development team that is strategically located throughout North America. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to company headquarters in Bend, Oregon and client sites as needed.  Preference will be given to those with international Business Development and Account Management experience for commercial manufacturing.  

    \n
    \n
     
    ","descriptionBodyPlain":"The Account Manager, Commercial Manufacturing will drive the expansion of Serán’s commercial manufacturing portfolio for oral solid drug products by identifying, qualifying, and securing high‑value opportunities. The Account Manager will serve as the primary point of contact for prospective and existing clients, guiding them from initial engagement through term sheet negotiation, commercial supply agreement execution, and ongoing account management. This role will ensure each opportunity aligns with Serán’s technical capabilities, service offerings, and strategic growth objectives. Primary responsibilities will be to maintain strong client relationships throughout the commercial manufacturing lifecycle to support successful project execution and optimize utilization of Serán’s commercial manufacturing capacity.  \nThis role will join a highly skilled Business Development team that is strategically located throughout North America. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to company headquarters in Bend, Oregon and client sites as needed.  Preference will be given to those with international Business Development and Account Management experience for commercial manufacturing.  \n \n","hostedUrl":"https://jobs.lever.co/seranbio/b15bf1de-133a-4861-be34-5f3598641c28","applyUrl":"https://jobs.lever.co/seranbio/b15bf1de-133a-4861-be34-5f3598641c28/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Non-exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Finance","allLocations":["Bend, Oregon"]},"createdAt":1780095259050,"descriptionPlain":"Serán BioScience is searching for an Accounting Coordinator to join the Finance and Accounting Department. This position will ensure complete and systematic accounting records of receipts and disbursements in the organization by performing complex data entry and monitoring tasks and applying accepted procedures in preparing and maintaining accounting records. The Accounting Coordinator will contribute to the accounting team, allowing for growth opportunities for those who desire additional training or dedicated responsibilities for those who prefer to be an independent contributor. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","description":"
    Serán BioScience is searching for an Accounting Coordinator to join the Finance and Accounting Department. This position will ensure complete and systematic accounting records of receipts and disbursements in the organization by performing complex data entry and monitoring tasks and applying accepted procedures in preparing and maintaining accounting records. The Accounting Coordinator will contribute to the accounting team, allowing for growth opportunities for those who desire additional training or dedicated responsibilities for those who prefer to be an independent contributor.
    \n
     
    \n
    Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.
    ","id":"df06ed0f-5c97-4581-8cd7-c09781c48023","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Conducts routine data entry management for accounting records including accounts payable, billing, accounts receivable, and bank account and credit card reconciliations
    • \n
  • Reviews billing statements, invoices, and similar documents for accuracy; alerts supervisory staff of any discrepancies
    • \n
  • Prepares and distributes financial and accounting reports
    • \n
  • Posts journal entries to general ledger
    • \n
  • Generates summary sheets for use by supervisor or auditor
    • \n
  • May assist in onboarding and cross-training additional staff
    • \n
  • Scope of work may increase to align with company initiatives
    • \n
  • Performs other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Thorough understanding of bookkeeping practices and procedures
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Ability to follow verbal and written instructions
    • \n
  • Ability to work independently and efficiently to meet deadlines
    • \n
  • Aptitude and attitude for process improvement
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Proficient in Microsoft Office Suite, particularly Excel
    • \n
  • High comfort level navigating enterprise software and banking portals
    • \n
  • Experience with SAP, Smartsheet, Rippling, and RAMP a significant advantage  
    • \n"},{"text":"Education and Experience ","content":"\n
  • High school diploma or equivalent required; Associate’s degree in Business or Accounting or some bookkeeping coursework/training preferred
    • \n
  • Minimum of two years of experience in Accounting
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting at a desk and working on a computer
    • \n
  • Must be able to lift 15 pounds at times
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Accounting Coordinator","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an Accounting Coordinator to join the Finance and Accounting Department. This position will ensure complete and systematic accounting records of receipts and disbursements in the organization by performing complex data entry and monitoring tasks and applying accepted procedures in preparing and maintaining accounting records. The Accounting Coordinator will contribute to the accounting team, allowing for growth opportunities for those who desire additional training or dedicated responsibilities for those who prefer to be an independent contributor.
    \n
     
    \n
    Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.
    ","descriptionBodyPlain":"Serán BioScience is searching for an Accounting Coordinator to join the Finance and Accounting Department. This position will ensure complete and systematic accounting records of receipts and disbursements in the organization by performing complex data entry and monitoring tasks and applying accepted procedures in preparing and maintaining accounting records. The Accounting Coordinator will contribute to the accounting team, allowing for growth opportunities for those who desire additional training or dedicated responsibilities for those who prefer to be an independent contributor. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","hostedUrl":"https://jobs.lever.co/seranbio/df06ed0f-5c97-4581-8cd7-c09781c48023","applyUrl":"https://jobs.lever.co/seranbio/df06ed0f-5c97-4581-8cd7-c09781c48023/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-time Exempt","department":"Quality","location":"Bend, Oregon","team":"Analytical Development","allLocations":["Bend, Oregon"]},"createdAt":1776902742175,"descriptionPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients.  The Scientist II role will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs.  The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high‑quality data that enables the success of early/late phase clinical programs.\n","description":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients.  The Scientist II role will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs.  The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high‑quality data that enables the success of early/late phase clinical programs.
    ","id":"8664ab0e-15f1-409a-9e53-450a791678a3","lists":[{"text":"Duties and Responsibilities","content":"\n
  • Perform analytical testing such as UHPLC/HPLC, KF, Water Activity, Dissolution to support small molecules drug product development in GMP environment
    • \n
  • Develop and optimize methods for drug products across early phase and late phase clinical stages
    • \n
  • Execute method transfers to QC or partner labs, ensuring robustness and compliance.
    • \n
  • Plan, troubleshoot, and independently execute laboratory studies, generating high‑quality data for CMC decision‑making.
    • \n
  • Prepare and review technical reports, analytical methods, and protocols, contributing to regulatory‑ready documentation.
    • \n
  • Collaborate with cross‑functional teams (QC, QA, Process Development, Project Management) and communicate results to internal and external stakeholders.
    • \n
  • Act as a subject matter expert (SME) in analytical development, providing technical leadership and supporting analytical strategy.
    • \n
  • Initiate, draft, and perform testing for discrepancy reports; as necessary.
    • \n
  • Maintain GMP training certification to be able to perform work in a GMP laboratory
    • \n
  • Provide regular updates to senior management on project progress
    • \n
  • Identify opportunities for process improvements and propose solutions
    • \n
  • Identifies out of trend data.
    • \n
  • Responsibilities may increase in scope to align with company initiatives.
    • \n"},{"text":"Required Skills/Abilities","content":"
    \n
    "},{"text":"Education and Experience","content":"
    \n
    "},{"text":"Physical Requirements","content":"
    \n
    "}],"text":"Analytical Development Scientist II","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients.  The Scientist II role will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs.  The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high‑quality data that enables the success of early/late phase clinical programs.
    ","descriptionBodyPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients.  The Scientist II role will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs.  The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high‑quality data that enables the success of early/late phase clinical programs.\n","hostedUrl":"https://jobs.lever.co/seranbio/8664ab0e-15f1-409a-9e53-450a791678a3","applyUrl":"https://jobs.lever.co/seranbio/8664ab0e-15f1-409a-9e53-450a791678a3/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Project Management","allLocations":["Bend, Oregon"]},"createdAt":1774051484125,"descriptionPlain":"The Associate Project Manager role with Seran Bioscience plays a crucial supporting role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines and supporting the internal teams, and for communicating directly with clients. Each project lifespan can be broken into 6 unique phases for which the Associate Project Manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. The Associate Project Manager is responsible for relaying critical project status and technical updates to Serán’s clients; highly developed communication and writing skills are expected. Those with technical industry experience who have an interest in growing their career into a client-facing or customer service role are encouraged to apply. \n","description":"
    \n

    The Associate Project Manager role with Seran Bioscience plays a crucial supporting role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines and supporting the internal teams, and for communicating directly with clients. Each project lifespan can be broken into 6 unique phases for which the Associate Project Manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. The Associate Project Manager is responsible for relaying critical project status and technical updates to Serán’s clients; highly developed communication and writing skills are expected. Those with technical industry experience who have an interest in growing their career into a client-facing or customer service role are encouraged to apply. 

    \n
    ","id":"303d1d66-174c-4b76-a5b2-b0c04b9b9529","lists":[{"text":"Duties and Responsibilities","content":"
    \n\n
  • Works closely with Project Managers to learn and apply internal processes and procedures for project development and execution
    • \n
  • Works to manage a portfolio of compounds simultaneously throughout different phases of development
    • \n
  • Serves as primary interface between the client and the Seran internal project team
    • \n
  • Facilitates information flow between internal teams and client for materials, shipments, documents, project updates, meeting agendas, and timelines
    • \n
  • Owns the overall project timeline, schedule, and resources
    • \n
  • Ensures internal teams are well informed on project timelines and goals, helps facilitate information transfer within internal teams
    • \n
  • Maintains consistent and accurate communication with the client via regularly scheduled and ad-hoc updates
    • \n
  • Communicates project execution to the client and schedules regular meetings, both internal and external, to review the execution of each project phase with the technical team
    • \n
  • Oversees and influences across departments to coordinate program support as needed
    • \n
  • Manages timeline, budget forecasting, resource planning, project meetings, document tracking, and owns the overall project progress
    • \n
  • Communicates risk internally and externally
    • \n
  • Ensures project milestones are communicated and met
    • \n
  • Acts as primary point of contact for external resources and client queries
    • \n
  • Schedules and coordinates project meetings both internally and externally
    • \n
  • Oversees, coordinates, and tracks shipments of all project/client materials
    • \n
  • Scope of work may increase to align with Company initiatives
    • \n
  • Performs other related duties as assigned 
    • \n\n
    "},{"text":"Required Knowledge and Skills","content":"
    \n
    \n
    \n
    "},{"text":"Education and Experience ","content":"
    \n
    "},{"text":"Physical Requirement ","content":"
    \n
    \n
    \n
    "}],"text":"Associate Project Manager","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    \n

    The Associate Project Manager role with Seran Bioscience plays a crucial supporting role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines and supporting the internal teams, and for communicating directly with clients. Each project lifespan can be broken into 6 unique phases for which the Associate Project Manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. The Associate Project Manager is responsible for relaying critical project status and technical updates to Serán’s clients; highly developed communication and writing skills are expected. Those with technical industry experience who have an interest in growing their career into a client-facing or customer service role are encouraged to apply. 

    \n
    ","descriptionBodyPlain":"The Associate Project Manager role with Seran Bioscience plays a crucial supporting role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines and supporting the internal teams, and for communicating directly with clients. Each project lifespan can be broken into 6 unique phases for which the Associate Project Manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. The Associate Project Manager is responsible for relaying critical project status and technical updates to Serán’s clients; highly developed communication and writing skills are expected. Those with technical industry experience who have an interest in growing their career into a client-facing or customer service role are encouraged to apply. \n","hostedUrl":"https://jobs.lever.co/seranbio/303d1d66-174c-4b76-a5b2-b0c04b9b9529","applyUrl":"https://jobs.lever.co/seranbio/303d1d66-174c-4b76-a5b2-b0c04b9b9529/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Business Development","allLocations":["Bend, Oregon"]},"createdAt":1772845966040,"descriptionPlain":"Serán is expanding the Business Development team and is searching for a BD Associate dedicated to inside sales. This role will be responsible for the growth of Serán’s business through managing the lead generation and progression process.  As part of the Business Operations team, the role will act as a key contributor supporting the Marketing, Business Development, Proposals and Project Management teams. \n \nThe position’s responsibilities include delivering market intelligence, prospect and target identification, and lead generation and follow-up.  This role acts as a point of contact with prospective customers, identifying and aligning their needs with internal capabilities and ensuring that potential clients are correctly introduced to Serán and our customer experience expectations.\n  \nThe position includes significant growth opportunities in the company with potential entry into Business development and Marketing roles. Those with direct industry experience in client-facing roles with an aptitude for expanding into a Business Development path are encouraged to apply.    \n","description":"
    Serán is expanding the Business Development team and is searching for a BD Associate dedicated to inside sales. This role will be responsible for the growth of Serán’s business through managing the lead generation and progression process.  As part of the Business Operations team, the role will act as a key contributor supporting the Marketing, Business Development, Proposals and Project Management teams. 
    \n
     
    \n
    The position’s responsibilities include delivering market intelligence, prospect and target identification, and lead generation and follow-up.  This role acts as a point of contact with prospective customers, identifying and aligning their needs with internal capabilities and ensuring that potential clients are correctly introduced to Serán and our customer experience expectations.
    \n
      
    \n
    The position includes significant growth opportunities in the company with potential entry into Business development and Marketing roles. Those with direct industry experience in client-facing roles with an aptitude for expanding into a Business Development path are encouraged to apply.    
    ","id":"116f67b9-8d07-4093-a7c6-0ab45d8d1347","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Engage with Leads follow up acting as Serán’s first point of contact, ensuring a positive customer experience and rapid feedback
    • \n
  • Generate and manage inbound lead follow up process from marketing, BD, and other sources
    • \n
  • Through market intelligence, create and prioritize client target and prospect lists based on Serán BD priorities
    • \n
  • Support the business development team coordination of cross-functional compilation of answers to RFIs and RFPs
    • \n\n\n
  • Understand Serán’s capabilities as a first evaluation of the project fit
    • \n
  • Qualify active leads to enable the BD team to advance leads to opportunities and ultimately new clients and projects
    • \n
  • Collaborate with Marketing and support marketing campaigns
    • \n
  • Coordinate with Serán’s SMEs to ensure capabilities are accurately and broadly promoted in the marketplace
    • \n
  • Support Serán’s Proposals team in ensuring the accuracy, quality and consistency of proposals are aligned with customer needs
    • \n
  • Work with business operations, project management, and scheduling teams to ensure that client timelines are achievable 
    • \n
  • Work with legal team to support establishing necessary CDA documents for initial project conversations
    • \n
  • Work with the business and technical leadership to continuously improve sales process and customer experience
    • \n
  • Work with the technical and business teams to evaluate pricing for new and existing equipment and processes
    • \n
  • Support field BD as a consultant to help customers select the best possible services for their needs
    • \n
  • Contribute to the maintaining of costing templates
    • \n
  • Perform timely CRM inputs critical to daily monitoring of business status
    • \n
  • May travel to and participates in trade and technical conferences
    • \n
  • Scope of responsibilities may increase to align with company initiatives
    • \n
  • Performs other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail 
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate 
    • \n
  • Excellent interpersonal and customer service skills
    • \n
  • Excellent sales and customer service skills
    • \n
  • Excellent time management skills with a proven ability to meet deadlines 
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Experience with CRM systems, especially Salesforce preferred
    • \n
  • Ability to function well in a high-paced and at times stressful environment 
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree in physical sciences or engineering in combination with;
    • \n
  • 3-5 years’ experience in a technical pharmaceutical development role 
    • \n
  • Experience interacting with customers and sales experience, preferred
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer.
    • \n\n
     
    "}],"text":"Business Development Associate, Inside Sales","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán is expanding the Business Development team and is searching for a BD Associate dedicated to inside sales. This role will be responsible for the growth of Serán’s business through managing the lead generation and progression process.  As part of the Business Operations team, the role will act as a key contributor supporting the Marketing, Business Development, Proposals and Project Management teams. 
    \n
     
    \n
    The position’s responsibilities include delivering market intelligence, prospect and target identification, and lead generation and follow-up.  This role acts as a point of contact with prospective customers, identifying and aligning their needs with internal capabilities and ensuring that potential clients are correctly introduced to Serán and our customer experience expectations.
    \n
      
    \n
    The position includes significant growth opportunities in the company with potential entry into Business development and Marketing roles. Those with direct industry experience in client-facing roles with an aptitude for expanding into a Business Development path are encouraged to apply.    
    ","descriptionBodyPlain":"Serán is expanding the Business Development team and is searching for a BD Associate dedicated to inside sales. This role will be responsible for the growth of Serán’s business through managing the lead generation and progression process.  As part of the Business Operations team, the role will act as a key contributor supporting the Marketing, Business Development, Proposals and Project Management teams. \n \nThe position’s responsibilities include delivering market intelligence, prospect and target identification, and lead generation and follow-up.  This role acts as a point of contact with prospective customers, identifying and aligning their needs with internal capabilities and ensuring that potential clients are correctly introduced to Serán and our customer experience expectations.\n  \nThe position includes significant growth opportunities in the company with potential entry into Business development and Marketing roles. Those with direct industry experience in client-facing roles with an aptitude for expanding into a Business Development path are encouraged to apply.    \n","hostedUrl":"https://jobs.lever.co/seranbio/116f67b9-8d07-4093-a7c6-0ab45d8d1347","applyUrl":"https://jobs.lever.co/seranbio/116f67b9-8d07-4093-a7c6-0ab45d8d1347/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Business Development","allLocations":["Bend, Oregon"]},"createdAt":1753391241433,"descriptionPlain":"The Director of Business Development is responsible for driving new customers and business growth for Serán’s customer accounts. This position will develop business relationships with respective client organizations and serve as lead point of contact for all client matters. The successful candidate will have a fundamental understanding of drug development and drug product technologies and services. The role requires building relationships with clients and ability to anticipate client needs, align solutions with needs for current and future proposals/business development, ensure deadlines are met for active on-going projects and proposals, and help customers realize success relative to collaborations with Serán both current and in the future. \nThis role will join a highly skilled Business Development team that is strategically located throughout North America. The chosen candidate will focus on new client relationships within regions with growth opportunity to enhance customer service support while strengthening existing business relationships. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to Bend, Oregon as needed.\nCurrently recruiting for multiple positions in the Northeast, Atlantic and Southern US Territories.\n","description":"

    The Director of Business Development is responsible for driving new customers and business growth for Serán’s customer accounts. This position will develop business relationships with respective client organizations and serve as lead point of contact for all client matters. The successful candidate will have a fundamental understanding of drug development and drug product technologies and services. The role requires building relationships with clients and ability to anticipate client needs, align solutions with needs for current and future proposals/business development, ensure deadlines are met for active on-going projects and proposals, and help customers realize success relative to collaborations with Serán both current and in the future.

    \n

    This role will join a highly skilled Business Development team that is strategically located throughout North America. The chosen candidate will focus on new client relationships within regions with growth opportunity to enhance customer service support while strengthening existing business relationships. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to Bend, Oregon as needed.

    \n
    \n

    Currently recruiting for multiple positions in the Northeast, Atlantic and Southern US Territories.

    \n
    ","id":"41cdd80f-288f-4454-9933-4eea237a9834","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Generate new leads and opportunities leveraging Serán’s and the incumbents network 
    • \n
  • Build solid, trusting, and measurable relationships with clients and companies while developing a complete understanding of client needs 
    • \n
  • Participate in client visits, regional and national trade shows, and conferences as required
    • \n
  • Manage both Serán’s existing pipeline and new business opportunities
    • \n
  • Manage communications between customer and internal teams and assist with management of team activities assigned to each of your customers
    • \n
  • Work with various internal stakeholders (e.g., Executive, Tech Ops, Project Mgmt, etc.) to build client relationships and improve customer results
    • \n
  • Contribute to the development of proposals and presentations for new business development materials
    • \n
  • Adeptly present Serán’s capabilities and value proposition to new clients
    • \n
  • Negotiate agreements as part of a team with BD, corporate, and legal leadership, including CDAs, MSAs, and commercial supply agreements
    • \n
  • Resolve client issues, complaints and anticipate key account improvements by way of project management guidance and outreach
    • \n
  • Identify market trends and customer needs, building a short/medium/long-term sales pipeline in accordance with targets
    • \n
  • Participate in site management team and planning meetings, including setting objectives and strategies as well as take accountability for implementation and results
    • \n
  • Support the broader BD team in developing new service offerings and analyzing market trends
    • \n
  • Assist in the coordination and implementation of marketing strategies, and delegate tasks that achieve strategic goals
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n
  • Additional related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent interpersonal, business, and customer service skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent negotiation skills, with ability follow-through on customer contracts/management
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Proficient with CRM, Office and other related software
    • \n"},{"text":"Education and Experience ","content":"\n
  • Minimum requirement of a Bachelor’s degree in a related scientific discipline
    • \n
  • 5+ years of experience in pharmaceutical industry
    • \n
  • 2+ years of experience in a client-facing capacity is ideal but additional training can be provided
    • \n
  • Track record of technical leadership, including technical conference and client presentations
    • \n"},{"text":"Physical and Travel Requirements","content":"\n
  • Approximately 25% travel required, and at times > 50% may be required
    • \n
  • Travel will be domestic, with potential for international travel
    • \n
  • Prolonged periods of sitting at a desk and working on a computer
    • \n
  • Must be able to lift to 15 pounds at a time
    • \n"}],"text":"Business Development Director (Regional)","country":"US","workplaceType":"remote","opening":"","openingPlain":"","descriptionBody":"

    The Director of Business Development is responsible for driving new customers and business growth for Serán’s customer accounts. This position will develop business relationships with respective client organizations and serve as lead point of contact for all client matters. The successful candidate will have a fundamental understanding of drug development and drug product technologies and services. The role requires building relationships with clients and ability to anticipate client needs, align solutions with needs for current and future proposals/business development, ensure deadlines are met for active on-going projects and proposals, and help customers realize success relative to collaborations with Serán both current and in the future.

    \n

    This role will join a highly skilled Business Development team that is strategically located throughout North America. The chosen candidate will focus on new client relationships within regions with growth opportunity to enhance customer service support while strengthening existing business relationships. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to Bend, Oregon as needed.

    \n
    \n

    Currently recruiting for multiple positions in the Northeast, Atlantic and Southern US Territories.

    \n
    ","descriptionBodyPlain":"The Director of Business Development is responsible for driving new customers and business growth for Serán’s customer accounts. This position will develop business relationships with respective client organizations and serve as lead point of contact for all client matters. The successful candidate will have a fundamental understanding of drug development and drug product technologies and services. The role requires building relationships with clients and ability to anticipate client needs, align solutions with needs for current and future proposals/business development, ensure deadlines are met for active on-going projects and proposals, and help customers realize success relative to collaborations with Serán both current and in the future. \nThis role will join a highly skilled Business Development team that is strategically located throughout North America. The chosen candidate will focus on new client relationships within regions with growth opportunity to enhance customer service support while strengthening existing business relationships. Successful candidates will have clear communication within pharmaceutical development and manufacturing and remain within their preferred region, but will require travel to Bend, Oregon as needed.\nCurrently recruiting for multiple positions in the Northeast, Atlantic and Southern US Territories.\n","hostedUrl":"https://jobs.lever.co/seranbio/41cdd80f-288f-4454-9933-4eea237a9834","applyUrl":"https://jobs.lever.co/seranbio/41cdd80f-288f-4454-9933-4eea237a9834/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Finance","allLocations":["Bend, Oregon"]},"createdAt":1779483563700,"descriptionPlain":"Founded in 2016, Serán provides our clients with integrated drug product development and manufacturing solutions.  Seràn takes a science-first approach, using early process optimization and cutting-edge technologies right from the start to overcome challenges for the most complex projects and ensure the efficient advancement of drugs to the clinic. Due to our clients’ success, Serán has grown to over 200 team members passionate about continuing our mission of pioneering innovation. A major expansion to the manufacturing campus is underway with over 100,000 sq/ft of commercial manufacturing to be complete in 2027.   \n \nSerán is seeking a Controller to add to their Finance team to support business growth. The Controller is primarily responsible for the accurate tracking and communication of Serán’s financial position, to inside and outside constituents. The controller will ensure that the Company’s financial outputs are (1) in line with Generally Accepted Accounting Principles and (2) informative to partners and stakeholders. Previous experience with cost accounting in a manufacturing environment will be prioritized.\n","description":"
    Founded in 2016, Serán provides our clients with integrated drug product development and manufacturing solutions.  Seràn takes a science-first approach, using early process optimization and cutting-edge technologies right from the start to overcome challenges for the most complex projects and ensure the efficient advancement of drugs to the clinic. Due to our clients’ success, Serán has grown to over 200 team members passionate about continuing our mission of pioneering innovation. A major expansion to the manufacturing campus is underway with over 100,000 sq/ft of commercial manufacturing to be complete in 2027.   
    \n
     
    \n
    Serán is seeking a Controller to add to their Finance team to support business growth. The Controller is primarily responsible for the accurate tracking and communication of Serán’s financial position, to inside and outside constituents. The controller will ensure that the Company’s financial outputs are (1) in line with Generally Accepted Accounting Principles and (2) informative to partners and stakeholders. Previous experience with cost accounting in a manufacturing environment will be prioritized.
    \n
     
    \n
    On-site preferred; however, will consider hybrid or remote work locations for candidates with proven ability to perform at the highest level of expectations and proficiency.    
    ","id":"0534643a-61bd-4918-99de-9156b4b0c524","lists":[{"text":"Supervisory Responsibilities","content":"
    \n\n
  • Oversees daily workflow of the department
    • \n
  • Mentors team to ensure redundancy of capabilities and development of talent
    • \n
  • Works with colleagues across the firm to educate partner departments on accounting/finance needs and directives
    • \n
  • Oversees accounting training program and identifies training needs
    • \n
  • Recruits, interviews, hires and trains new staff
    • \n
  • Provides constructive and timely performance evaluations
    • \n
  • Handles discipline and termination of employees in accordance with company policy
    • \n\n
    "},{"text":"Duties & Responsibilities","content":"
    \n\n
  • Planning, directing, and coordinating all accounting operational functions
    • \n
  • Maintaining and improving internal controls\n
    • "},{"text":"Required Skills and Experience","content":"
    \n\n
  • Solid working knowledge of all aspects of generally accepted accounting principles (GAAP)
    • \n
  • Ability to close a monthly period’s financial results and presentation without difficulty
    • \n
  • Strong facility with usage, design, and improvement of accounting software and enterprise systems.  SAP experience a strong advantage
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Exceptional mentoring skills
    • \n
  • Highest integrity and ability to keep company confidences
    • \n
  • Excellent written and verbal communication skills
    • \n
  • Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs
    • \n
  • Exceptional Excel skills and facility with software related to all accounting functions: payroll, AP, AR, time keeping, banking, project management, etc.
    • \n\n
    "},{"text":"Education and Experience","content":"
    \n
    "},{"text":"Physical Requirements","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Adheres to consistent and predicable work schedule
    • \n\n
    "}],"text":"Controller","country":"US","workplaceType":"hybrid","opening":"","openingPlain":"","descriptionBody":"
    Founded in 2016, Serán provides our clients with integrated drug product development and manufacturing solutions.  Seràn takes a science-first approach, using early process optimization and cutting-edge technologies right from the start to overcome challenges for the most complex projects and ensure the efficient advancement of drugs to the clinic. Due to our clients’ success, Serán has grown to over 200 team members passionate about continuing our mission of pioneering innovation. A major expansion to the manufacturing campus is underway with over 100,000 sq/ft of commercial manufacturing to be complete in 2027.   
    \n
     
    \n
    Serán is seeking a Controller to add to their Finance team to support business growth. The Controller is primarily responsible for the accurate tracking and communication of Serán’s financial position, to inside and outside constituents. The controller will ensure that the Company’s financial outputs are (1) in line with Generally Accepted Accounting Principles and (2) informative to partners and stakeholders. Previous experience with cost accounting in a manufacturing environment will be prioritized.
    \n
     
    \n
    On-site preferred; however, will consider hybrid or remote work locations for candidates with proven ability to perform at the highest level of expectations and proficiency.    
    ","descriptionBodyPlain":"Founded in 2016, Serán provides our clients with integrated drug product development and manufacturing solutions.  Seràn takes a science-first approach, using early process optimization and cutting-edge technologies right from the start to overcome challenges for the most complex projects and ensure the efficient advancement of drugs to the clinic. Due to our clients’ success, Serán has grown to over 200 team members passionate about continuing our mission of pioneering innovation. A major expansion to the manufacturing campus is underway with over 100,000 sq/ft of commercial manufacturing to be complete in 2027.   \n \nSerán is seeking a Controller to add to their Finance team to support business growth. The Controller is primarily responsible for the accurate tracking and communication of Serán’s financial position, to inside and outside constituents. The controller will ensure that the Company’s financial outputs are (1) in line with Generally Accepted Accounting Principles and (2) informative to partners and stakeholders. Previous experience with cost accounting in a manufacturing environment will be prioritized.\n","hostedUrl":"https://jobs.lever.co/seranbio/0534643a-61bd-4918-99de-9156b4b0c524","applyUrl":"https://jobs.lever.co/seranbio/0534643a-61bd-4918-99de-9156b4b0c524/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1776727671606,"descriptionPlain":"The Director of Commercial Quality Assurance plays an integral role in fostering a culture of quality, efficiency, and excellence, ensuring that quality and compliance are integrated into the day-to-day operations and long-term Quality strategy.  The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway, giving the selected candidate the ability to truly be a visionary leader in the development and implementation of the Commercial Quality Assurance program. This position will provide strategic direction and guidance for the Quality Assurance functions to assure end-to-end harmonization of quality processes including risk and GMP core management, and regulatory compliance with worldwide requirements. The position is also responsible for ensuring that Quality operates in compliance within internal quality system procedures, mitigation of identified compliance and quality risks throughout product life cycle from development to commercialization for the products manufactured at Serán BioScience. \n","description":"

    The Director of Commercial Quality Assurance plays an integral role in fostering a culture of quality, efficiency, and excellence, ensuring that quality and compliance are integrated into the day-to-day operations and long-term Quality strategy.  The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway, giving the selected candidate the ability to truly be a visionary leader in the development and implementation of the Commercial Quality Assurance program. This position will provide strategic direction and guidance for the Quality Assurance functions to assure end-to-end harmonization of quality processes including risk and GMP core management, and regulatory compliance with worldwide requirements. The position is also responsible for ensuring that Quality operates in compliance within internal quality system procedures, mitigation of identified compliance and quality risks throughout product life cycle from development to commercialization for the products manufactured at Serán BioScience.

    ","id":"1767bb77-4865-4575-9b2b-b0e962ccc054","lists":[{"text":"Duties and Responsibilities","content":"\n
  • Identifies and eliminates risk to continuously improve customer satisfaction and product reliability
    • \n
  • Leads and steers Quality Assurance (QA) Department, including hires and mentors QA personnel, provides constructive and timely performance evaluations, and handles discipline of employees in accordance with company policy
    • \n
  • Leads implementation and continuous improvement of the company’s quality systems and facility validation
    • \n
  • Creates product quality documentation system by writing and updating quality assurance procedures
    • \n
  • Leads Quality System improvements, Investigations, CAPAs, Change Management, Document Control, Validation, and Auditing
    • \n
  • Responsible for oversight of site activities, assuring that products are manufactured in compliance with cGMP, FDA, and EU guidelines       
    • \n
  • Documents authorship, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
    • \n
  • Supports internal audits, client audits and regulatory inspections
    • \n
  • Provides support and oversight of Quality Management Review meetings
    • \n
  • Oversight of a broad range of documentation including, but not limited to User Requirements Specifications (URS), Functional and Design Specifications, Testing Protocols (IQ/OQ/PQ), Change Controls, and Risk Assessments
    • \n
  • Maintains product quality by enforcing quality assurance policies and procedures and government requirements
    • \n
  • Collaborates with other members of management to develop new product and engineering designs and manufacturing and training methods
    • \n
  • Prepares product and process quality reports by collecting, analyzing, and summarizing information and trends
    • \n
  • Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate in manufacturing and QC
    • \n
  • Manages the QA budget to ensure that resources are allocated appropriately and that all projects are completed on time and within budget
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n
  • Other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • General knowledge of oral solid dosage manufacturing processes
    • \n
  • Experience with Commercial Manufacturing oversight, with a preference for those who have built and developed programs
    • \n
  • Expert knowledge of GMP guidelines and Quality expectations for late-phase and commercial programs
    • \n
  • In-depth understanding and application of cGMP principles, concepts, practices, and standards
    • \n
  • Experience with regulatory inspections by the FDA and EU authorities
    • \n
  • Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally
    • \n
  • Demonstrated ability to partner with other functional groups to achieve business objectives
    • \n
  • Broad knowledge of FDA and international regulations related to GMPs and Pharmaceuticals
    • \n
  • Experience organizing and managing work responsibilities while working independently with minimal oversight
    • \n
  • Time and project management skills with the ability to multi-task and meet deadlines
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Proven ability to lead organizations
    • \n
  • Ability to prioritize tasks and to delegate when appropriate 
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree in a scientific discipline; advanced degree is preferred.
    • \n
  • Requires a minimum of 15 years of GMP and Quality experience in the Pharmaceutical or Biotechnology industry
    • \n
  • Requires a minimum of 10 years in a QA management role
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at a time
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Director of Commercial Quality Assurance","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"

    The Director of Commercial Quality Assurance plays an integral role in fostering a culture of quality, efficiency, and excellence, ensuring that quality and compliance are integrated into the day-to-day operations and long-term Quality strategy.  The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway, giving the selected candidate the ability to truly be a visionary leader in the development and implementation of the Commercial Quality Assurance program. This position will provide strategic direction and guidance for the Quality Assurance functions to assure end-to-end harmonization of quality processes including risk and GMP core management, and regulatory compliance with worldwide requirements. The position is also responsible for ensuring that Quality operates in compliance within internal quality system procedures, mitigation of identified compliance and quality risks throughout product life cycle from development to commercialization for the products manufactured at Serán BioScience.

    ","descriptionBodyPlain":"The Director of Commercial Quality Assurance plays an integral role in fostering a culture of quality, efficiency, and excellence, ensuring that quality and compliance are integrated into the day-to-day operations and long-term Quality strategy.  The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway, giving the selected candidate the ability to truly be a visionary leader in the development and implementation of the Commercial Quality Assurance program. This position will provide strategic direction and guidance for the Quality Assurance functions to assure end-to-end harmonization of quality processes including risk and GMP core management, and regulatory compliance with worldwide requirements. The position is also responsible for ensuring that Quality operates in compliance within internal quality system procedures, mitigation of identified compliance and quality risks throughout product life cycle from development to commercialization for the products manufactured at Serán BioScience. \n","hostedUrl":"https://jobs.lever.co/seranbio/1767bb77-4865-4575-9b2b-b0e962ccc054","applyUrl":"https://jobs.lever.co/seranbio/1767bb77-4865-4575-9b2b-b0e962ccc054/apply"},{"additionalPlain":"","additional":"
    \n
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Manufacturing Operations","location":"Bend, Oregon","team":"Environmental Health & Safety","allLocations":["Bend, Oregon"]},"createdAt":1779483261468,"descriptionPlain":"","description":"

    Serán BioScience is searching for a strategic leader to build and steer the EHS team. The EHS Director is responsible for developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for employees.  This role will shape and drive programs that safeguard employees, facilities, and the environment, ensuring regulatory compliance in fast-paced, high-stakes CDMO operations. Looking for a leader with expertise to help guide the safe handling of novel drug therapeutics while fostering a culture of risk awareness and operational excellence.  As a partner in the planning and execution of a greenfield commercial manufacturing site, this role will influence facility design, manufacturing projects, and process improvements, integrating modern safety protocols and digital tools.  Ideal candidates bring a strong technical foundation, certifications like CSP or CIH, and a decade of experience in EHS leadership within regulated manufacturing environments. By joining a CDMO as its Director of EHS, you will play a pivotal role in protecting people and products, building a resilient safety culture, and contributing to the delivery of life-changing therapies worldwide. 

    ","id":"5fa284f9-cb0d-4f89-9ec5-6862d66159e4","lists":[{"text":"","content":"
    \n
    "},{"text":"Required Skills and Abilities ","content":"
    \n
    \n
    \n
    "},{"text":"Education and Experience ","content":"
    \n
    \n\n
  • Bachelor’s degree in Environmental Science, Occupational Health and Safety, or equivalent combination of education and/or experience
    • \n
  • Proven experience (10+ years) is EHS, preferably within biopharma or pharmaceutical industry
    • \n
  • 5+ years of successful EH&S leadership experience directly managing EH&S staff
    • \n
  • Successful experience in leading teams in a multi-plant and/or multi-site cGMP-regulated commercial manufacturing environment, including cross-functional team leadership
    • \n
  • In-depth knowledge of EHS regulations and standards, including OSHA, EPA, and other relevant agencies
    • \n
  • Professional certifications such as Certified Safety Professional (CSP) or Certified Industrial Hygienist (CIH) are preferred 
    • \n\n
    \n
    "},{"text":"Physical Requirements ","content":"
    \n
    \n
    \n
    \n
    \n
    "}],"text":"Director of Environmental Health and Safety","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"

    Serán BioScience is searching for a strategic leader to build and steer the EHS team. The EHS Director is responsible for developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for employees.  This role will shape and drive programs that safeguard employees, facilities, and the environment, ensuring regulatory compliance in fast-paced, high-stakes CDMO operations. Looking for a leader with expertise to help guide the safe handling of novel drug therapeutics while fostering a culture of risk awareness and operational excellence.  As a partner in the planning and execution of a greenfield commercial manufacturing site, this role will influence facility design, manufacturing projects, and process improvements, integrating modern safety protocols and digital tools.  Ideal candidates bring a strong technical foundation, certifications like CSP or CIH, and a decade of experience in EHS leadership within regulated manufacturing environments. By joining a CDMO as its Director of EHS, you will play a pivotal role in protecting people and products, building a resilient safety culture, and contributing to the delivery of life-changing therapies worldwide. 

    ","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/seranbio/5fa284f9-cb0d-4f89-9ec5-6862d66159e4","applyUrl":"https://jobs.lever.co/seranbio/5fa284f9-cb0d-4f89-9ec5-6862d66159e4/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1776197236416,"descriptionPlain":"Serán BioScience seeks a Director, Quality Engineering & Computer System Assurance (CSA) to oversee and provide strategic and operational leadership for the organization’s validation, qualification, and computerized systems assurance programs.  This role will support GMP manufacturing, laboratory, and quality systems that stretch across clinical and commercial operations.\n \nThis position is responsible for establishing and maintaining a risk-based validation and CSA framework ensuring that facilities, utilities, equipment, analytical methods, processes, and computerized systems remain in a validated state throughout their lifecycle. The Director, Quality Engineering & CSA ensures all validation and data integrity activities comply with FDA, EU, and international regulatory requirements, including cGMP, GAMP guidance, and current regulatory expectations for data integrity.\n \nThe role partners with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to ensure validated systems and processes enable safe, compliant, and reliable manufacturing of clinical and commercial products. The Director, Quality Engineering & CSA also serves as a key Quality leader during regulatory inspections, client audits, and internal quality reviews, and drives continuous improvement initiatives related to validation lifecycle management, computerized system assurance, and data governance.\n","description":"
    Serán BioScience seeks a Director, Quality Engineering & Computer System Assurance (CSA) to oversee and provide strategic and operational leadership for the organization’s validation, qualification, and computerized systems assurance programs.  This role will support GMP manufacturing, laboratory, and quality systems that stretch across clinical and commercial operations.
    \n
     
    \n
    This position is responsible for establishing and maintaining a risk-based validation and CSA framework ensuring that facilities, utilities, equipment, analytical methods, processes, and computerized systems remain in a validated state throughout their lifecycle. The Director, Quality Engineering & CSA ensures all validation and data integrity activities comply with FDA, EU, and international regulatory requirements, including cGMP, GAMP guidance, and current regulatory expectations for data integrity.
    \n
     
    \n
    The role partners with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to ensure validated systems and processes enable safe, compliant, and reliable manufacturing of clinical and commercial products. The Director, Quality Engineering & CSA also serves as a key Quality leader during regulatory inspections, client audits, and internal quality reviews, and drives continuous improvement initiatives related to validation lifecycle management, computerized system assurance, and data governance.
    ","id":"d2ef8cf2-75af-482b-b330-3e9a4fbf5b35","lists":[{"text":"Duties and Responsibilities ","content":"
    Strategic Leadership
    \n\n
  • Develops and implements the site strategy for Quality Engineering and Computer System Assurance(CSA) programs
    • \n
  • Supports the establishment governance structures for risk-based validation lifecycle management including planning, execution, maintenance, and periodic review
    • \n
  • Leads initiatives to modernize validation practices including CSA adoption, digital validation approaches, and automation lifecycle management
    • \n
  • Defines key performance indicators (KPIs) and metrics to measure effectiveness of QualityEngineering and CSA programs
    • \n
  • Provides leadership to cross-functional teams supporting validation, qualification, and system lifecycle activitie
    • \n\n
    Validation Lifecycle Oversight
    \n\n
  • Provides Quality leadership and oversight of validation programs including:\n\n
  • Facility, utility, and equipment qualification, Cleaning validation, Computerized systems validation / assurance, & Manufacturing automation systems
    • \n\n\n\n
    Key activities include:
    \n\n
  • Approval and oversight of validation lifecycle documentation including: \n\n
  • Validation Master Plans (VMP), User Requirement Specifications (URS), Functional and Design Specifications, Risk assessments, IQ/OQ/PQ protocols and reports, & Validation summary reports
    • \n\n\n
  • Ensures validation activities comply with internal procedures and regulatory requirements and remain aligned with the site Validation Master Plan
    • \n
  • Provides quality oversight for commissioning, qualification, and validation activities in highly automated manufacturing environments
    • \n
  • Ensures validated systems maintain a continuous state of control throughout their operational lifecycle
    • \n\n
    Computer System Assurance (CSA) & Data Integrity
    \n\n
  • Supports the design and implementation of the organization’s Computer System Assurance (CSA) and Computerized System Validation (CSV) programs
    • \n
  • Ensures computerized systems comply with data integrity principles (ALCOA++) and regulatory expectations
    • \n
  • Oversees validation lifecycle management for computerized systems including:\n\n
  • Manufacturing Execution Systems (MES), Laboratory Information Management Systems (LIMS), Quality management systems, Electronic Batch Record Systems, & Enterprise resource planning systems
    • \n\n\n
  • Implements risk-based testing approaches consistent with GAMP 5 and modern CSA methodologies
    • \n
  • Leads initiatives to strengthen enterprise data integrity governance programs across manufacturing, laboratory, and quality systems
    • \n
  • Supports system lifecycle activities including system upgrades, migrations, and decommissioning
    • \n\n
    Operational Quality Engineering Support
    \n\n
  • Provides QA oversight and approval for quality system elements impacting validated systems including:\n\n
  • Change control processes impacting validated systems and processes, Deviation and investigation management, Corrective and Preventive Actions (CAPA), Risk management and impact assessments, & Periodic reviews of validated systems
    • \n\n\n
  • Ensures that validation and CSA programs remain aligned with corporate policies, regulatory guidance, and evolving industry standards
    • \n
  • Provides QA support for technology transfer, new product introductions, and site capital projects
    • \n
  • Serves as the Quality Engineering representative for site project teams implementing new equipment, systems, or manufacturing technologies
    • \n
  • Supports troubleshooting of complex process or system issues impacting validated systems
    • \n
  • Serve as subject matter expert for validation, computerized systems assurance, and data integrity during regulatory inspections and Client audits
    • \n
  • Leads preparation and inspection readiness programs related to validation and data integrity
    • \n\n
    Leadership & People Management
    \n\n
  • Leads and develops a high-performing Quality Engineering and CSA organization
    • \n
  • Provides mentoring, coaching, and professional development for technical staff
    • \n
  • Establish clear departmental goals aligned with organizational quality and operational objectives
    • \n
  • Conducts performance reviews and ensure staff maintain appropriate training and GMP qualifications
    • \n
  • Fosters a culture of quality ownership, compliance, and continuous improvement
    • \n"},{"text":"Required Knowledge and Skills","content":"\n
  • Broad knowledge of FDA and international regulations related to GMPs and Pharmaceuticals
    • \n
  • Experience organizing and managing work responsibilities while working independently with minimal oversight
    • \n
  • Deep expertise in Computer System Validation / Computer System Assurance
    • \n
  • Validation lifecycle management, Data integrity regulations and industry guidance, Risk-based validation methodologies
    • \n
  • Time and project management skills with the ability to multi-task and meet deadlines
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Excellent interpersonal and customer service skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Strong supervisory and leadership skills
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Willingness to accept feedback from a variety of sources
    • \n
  • Ability to constructively manage conflict
    • \n
  • Ability to collaborate and work in cross-functional teams
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Ability to maintain productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree, preferably in a scientific discipline. Preference will be given to those with an advanced degree 
    • \n
  • Minimum of 10+ years previous GMP and Quality experience in the Pharmaceutical or Biotechnology industry
    • \n
  • Minimum of 5+ years previous experience with qualification/validation/CSA activities in a QA or Technical capacity
    • \n
  • Demonstrated experience with regulatory inspections by the FDA and EU authorities
    • \n"},{"text":"Physical Requirements ","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Adheres to consistent and predictable in-person attendance 
    • \n\n
    "}],"text":"Director, Quality Engineering & Computer System Assurance","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience seeks a Director, Quality Engineering & Computer System Assurance (CSA) to oversee and provide strategic and operational leadership for the organization’s validation, qualification, and computerized systems assurance programs.  This role will support GMP manufacturing, laboratory, and quality systems that stretch across clinical and commercial operations.
    \n
     
    \n
    This position is responsible for establishing and maintaining a risk-based validation and CSA framework ensuring that facilities, utilities, equipment, analytical methods, processes, and computerized systems remain in a validated state throughout their lifecycle. The Director, Quality Engineering & CSA ensures all validation and data integrity activities comply with FDA, EU, and international regulatory requirements, including cGMP, GAMP guidance, and current regulatory expectations for data integrity.
    \n
     
    \n
    The role partners with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to ensure validated systems and processes enable safe, compliant, and reliable manufacturing of clinical and commercial products. The Director, Quality Engineering & CSA also serves as a key Quality leader during regulatory inspections, client audits, and internal quality reviews, and drives continuous improvement initiatives related to validation lifecycle management, computerized system assurance, and data governance.
    ","descriptionBodyPlain":"Serán BioScience seeks a Director, Quality Engineering & Computer System Assurance (CSA) to oversee and provide strategic and operational leadership for the organization’s validation, qualification, and computerized systems assurance programs.  This role will support GMP manufacturing, laboratory, and quality systems that stretch across clinical and commercial operations.\n \nThis position is responsible for establishing and maintaining a risk-based validation and CSA framework ensuring that facilities, utilities, equipment, analytical methods, processes, and computerized systems remain in a validated state throughout their lifecycle. The Director, Quality Engineering & CSA ensures all validation and data integrity activities comply with FDA, EU, and international regulatory requirements, including cGMP, GAMP guidance, and current regulatory expectations for data integrity.\n \nThe role partners with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to ensure validated systems and processes enable safe, compliant, and reliable manufacturing of clinical and commercial products. The Director, Quality Engineering & CSA also serves as a key Quality leader during regulatory inspections, client audits, and internal quality reviews, and drives continuous improvement initiatives related to validation lifecycle management, computerized system assurance, and data governance.\n","hostedUrl":"https://jobs.lever.co/seranbio/d2ef8cf2-75af-482b-b330-3e9a4fbf5b35","applyUrl":"https://jobs.lever.co/seranbio/d2ef8cf2-75af-482b-b330-3e9a4fbf5b35/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Manufacturing Operations","location":"Bend, Oregon","team":"Environmental Health & Safety","allLocations":["Bend, Oregon"]},"createdAt":1779486336339,"descriptionPlain":"Serán BioScience is searching for an Environmental Health and Safety Manager to lead the EHS Department. This role is responsible for developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for all Serán employees. It's an exciting time to join this department, as the EHS Manager will be a key contributor for the future commercial manufacturing site while supporting EHS programs and initiatives across the company. Qualified applicants must have at least 10 years of EHS experience, with preference given to those within pharmaceutical or similar industries. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","description":"
    Serán BioScience is searching for an experienced Environmental Health and Safety Specialist to support the EHS Department. This role will assist in developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for all Serán employees. It's an exciting time to join this department, as the EHS Specialist will be a key contributor for the future commercial manufacturing site while supporting EHS programs and initiatives across the company. Qualified applicants must have at least 3-5 years of EHS experience, with preference given to those within pharmaceutical or similar industries. 
    \n
     
    \n
    Title and compensation will be commensurate with experience.  All EHS professional that meet the minimum qualifications are encouraged to apply.  Preference will be given to applicants with industry experience.  
    ","id":"ee9f4d1e-7eea-4052-bf21-4fca502ab79d","lists":[{"text":"Duties and Responsibilities ","content":"
    \n
    \n
    \n
    "},{"text":"Required Knowledge and Skills ","content":"\n
  • Demonstrates basic knowledge of related areas such as core safety and Environmental regulations, specifically those applicable to GMP and non-GMP manufacturing environments
    • \n
  • Demonstrates the ability to contribute where needed and manage competing priorities while executing on deliverables
    • \n
  • Showcases working knowledge of best practices in EHS and understands how safety integrates with other business areas
    • \n
  • Comprehends relevant regulations, codes, and consensus standards (OSHA, DOT, NIOSH, ACGIH), along with hands-on experience in risk assessment and exposure monitoring 
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Excellent time management skills with a proven ability to meet deadlines and delegate appropriate tasks
    • \n
  • Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions
    • \n
  • Demonstrates strong public speaking and training skills
    • \n
  • Proven ability to supervise and lead teams  
    • \n
  • Ability to function well in a high-paced and at times stressful environment. 
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Proficient with Microsoft Office Suite or related software with the aptitude to learn electronic EHS Management software
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree in Environmental Science, Occupational Health and Safety, or relevant field
    • \n
  • Specialist II: Minimum of 3 years of relevant experience in EHS, preferably within biopharma or pharmaceutical industry
    • \n
  • Specialist III: Minimum of 5 years of relevant experience in EHS, preferably within biopharma or pharmaceutical industry
    • \n
  • In-depth knowledge of EHS regulations and standards, including OSHA, EPA, and other relevant agencies
    • \n
  • Professional certifications such as Certified Safety Professional (CSP) or Certified Industrial Hygienist (CIH) are preferred
    • \n"},{"text":"Physical Requirement ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 55 pounds at times
    • \n
  • Must be able to operate a forklift and scissor lift
    • \n
  • Must be able to manipulate 55-gallon drums on drum dollies or with a hand truck
    • \n
  • Must be able to wear a respirator
    • \n
  • Ability to walk, stand, and climb in industrial environments for extended periods
    • \n
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"EHS Specialist II/III","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an experienced Environmental Health and Safety Specialist to support the EHS Department. This role will assist in developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for all Serán employees. It's an exciting time to join this department, as the EHS Specialist will be a key contributor for the future commercial manufacturing site while supporting EHS programs and initiatives across the company. Qualified applicants must have at least 3-5 years of EHS experience, with preference given to those within pharmaceutical or similar industries. 
    \n
     
    \n
    Title and compensation will be commensurate with experience.  All EHS professional that meet the minimum qualifications are encouraged to apply.  Preference will be given to applicants with industry experience.  
    ","descriptionBodyPlain":"Serán BioScience is searching for an Environmental Health and Safety Manager to lead the EHS Department. This role is responsible for developing, implementing, and overseeing all aspects of the environmental health and safety programs to ensure compliance with regulatory requirements and promote a safe and sustainable work environment for all Serán employees. It's an exciting time to join this department, as the EHS Manager will be a key contributor for the future commercial manufacturing site while supporting EHS programs and initiatives across the company. Qualified applicants must have at least 10 years of EHS experience, with preference given to those within pharmaceutical or similar industries. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","hostedUrl":"https://jobs.lever.co/seranbio/ee9f4d1e-7eea-4052-bf21-4fca502ab79d","applyUrl":"https://jobs.lever.co/seranbio/ee9f4d1e-7eea-4052-bf21-4fca502ab79d/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Process and Product Development","location":"Bend, Oregon","team":"Process and Product Development","allLocations":["Bend, Oregon"]},"createdAt":1777065938516,"descriptionPlain":"Serán is hiring for an Engineer I supporting Process Development who will support process development of pharmaceutical drug products beginning with initial prototyping experiments through early clinical manufacturing with guidance from senior team members.  Over time, the candidate will gain skills to support process design and scale-up, culminating in late stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis.  The Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","description":"
    \n

    Serán is hiring for an Engineer I supporting Process Development who will support process development of pharmaceutical drug products beginning with initial prototyping experiments through early clinical manufacturing with guidance from senior team members.  Over time, the candidate will gain skills to support process design and scale-up, culminating in late stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis.  The Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.

    \n
    ","id":"bad62924-319f-405d-934c-43762f69b4ee","lists":[{"text":"Duties and Responsibilities","content":"
    \n\n
  • Follows written protocols to execute basic and advanced procedures such as analytical protocols, laboratory experiments, or manufacturing processes
    • \n
  • Develops experimental protocols and templates with guidance
    • \n
  • Identifies out of trend data and proposes hypothesis and next steps with guidance
    • \n
  • Summarizes, reports, and analyzes data to draw conclusions with guidance
    • \n
  • Contributes to laboratory, instrument, and/or equipment maintenance and coordination
    • \n
  • Communicates technical information to internal team
    • \n
  • Communicates technical information to external partners with guidance
    • \n
  • Participates as technical lead in project teams with guidance
    • \n
  • Contributes to technical reports and presentations with guidance
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n\n
    "},{"text":"Required Skills and Abilities","content":"
    \n\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Ability to work collaboratively in a cross-functional team environment
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Experience with basic laboratory skills
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Accepts and addresses feedback from a variety of sources and constructively manages conflict
    • \n\n
    "},{"text":"Education and Experience","content":"
    \n\n
  • B.S. or higher in Science or Engineering discipline
    • \n\n
    "},{"text":"Physical Requirements","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 25 pounds regularly and up to 50 pounds occasionally
    • \n
  • Motor skills required for basic laboratory operations (pouring liquids, using utensils to transfer powders, visual assessments)
    • \n\n
    "}],"text":"Engineer I","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    \n

    Serán is hiring for an Engineer I supporting Process Development who will support process development of pharmaceutical drug products beginning with initial prototyping experiments through early clinical manufacturing with guidance from senior team members.  Over time, the candidate will gain skills to support process design and scale-up, culminating in late stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis.  The Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.

    \n
    ","descriptionBodyPlain":"Serán is hiring for an Engineer I supporting Process Development who will support process development of pharmaceutical drug products beginning with initial prototyping experiments through early clinical manufacturing with guidance from senior team members.  Over time, the candidate will gain skills to support process design and scale-up, culminating in late stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis.  The Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","hostedUrl":"https://jobs.lever.co/seranbio/bad62924-319f-405d-934c-43762f69b4ee","applyUrl":"https://jobs.lever.co/seranbio/bad62924-319f-405d-934c-43762f69b4ee/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-time Exempt","department":"Information Technology","location":"Bend, Oregon","team":"IT","allLocations":["Bend, Oregon"]},"createdAt":1780696295809,"descriptionPlain":"","description":"
    \n
    Serán is seeking an Operational Technologies Specialist who will be responsible for the management, maintenance, and deployment of laboratory and manufacturing systems across both GMP-regulated and development environments. This role partners closely with IT, Quality Assurance (QA), laboratory staff, and manufacturing teams to ensure seamless integration of technology solutions that enhance productivity, quality, data integrity, and operational efficiency.
    \n
    ","id":"06f08e9a-2978-451d-80d8-fe02e8638ca0","lists":[{"text":"Duties and Responsibilties","content":"
    \n\n
  • Administration and end user support for systems such as FTIR, Waters CDS, ELN, various manufacturing equipment, etc.
    • \n
  • Primary point of contact between users, internal IT and vendors
    • \n
  • Support lifecycle management of lab and manufacturing systems
    • \n
  • Work with management and subject matter experts to improve, develop and test existing applications and systems
    • \n
  • Identify and drive enhancements to existing systems and processes
    • \n
  • Support qualifications activities such as drafting, executing and or reviewing IOP/Q documentation
    • \n
  • Drafting SOP’s
    • \n
  • Manage and or support system and data backups for all OT system
    • \n
  • Ensure security, compliance and integrity of all data
    • \n
  • Support vital commissioning and qualification of systems is completed in alignment with site cGMP requirements
    • \n
  • May interact with regulatory and or client inspectors as necessary
    • \n
  • Provide support to reduce production downtime
    • \n
  • Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies
    • \n
  • Participates in process improvement and other non-routine projects
    • \n
  • Regularly interfaces with department stakeholders on technical and coordinative matters 
    • \n
  • Demonstrates cross-functional support capabilities with other teams
    • \n
  • Coordinate and oversee vendors and service providers
    • \n\n
    "},{"text":"Required Skills and Abilities","content":"
    \n\n
  • Strong working knowledge of on-premises and cloud-based IT infrastructures and operations best practices
    • \n
  • Excellent working knowledge of computer systems, network and systems administration, data storage systems, and security
    • \n
  • Excellent verbal, written, and interpersonal communication skills
    • \n
  • Ability to work independently or as a contributing team member
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Strong project management skills
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
    • \n
  • Follow detailed written and oral instructions 
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Strong time management skills with a proven ability to meet deadlines
    • \n
  • Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs 
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict  
    • \n
  • Ability to prioritize tasks and to keep leadership apprised of performance to timelines
    • \n
  • Proficient with Microsoft Office Suite
    • \n\n
    "},{"text":"Education and Experience","content":"
    \n
    "},{"text":"Physical Requirements","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer 
    • \n
  • Must be able to demonstrate mobility throughout multiple campus buildings   
    • \n
  • Must be able to lift up to 15 pounds at times routinely, 30 pounds occasionally.   
    • \n
  • Installing and monitoring equipment requires reaching overhead, kneeling, and crouching
    • \n\n
    "}],"text":"Operational Technologies Specialist","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    \n
    Serán is seeking an Operational Technologies Specialist who will be responsible for the management, maintenance, and deployment of laboratory and manufacturing systems across both GMP-regulated and development environments. This role partners closely with IT, Quality Assurance (QA), laboratory staff, and manufacturing teams to ensure seamless integration of technology solutions that enhance productivity, quality, data integrity, and operational efficiency.
    \n
    ","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/seranbio/06f08e9a-2978-451d-80d8-fe02e8638ca0","applyUrl":"https://jobs.lever.co/seranbio/06f08e9a-2978-451d-80d8-fe02e8638ca0/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Non-exempt","department":"Manufacturing Operations","location":"Bend, Oregon","team":"Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1779204563769,"descriptionPlain":"Serán BioScience is looking for dedicated individuals who are looking to learn how to become Operations Technicians and Operations Specialists. You will play an integral role in operating and maintaining specialized equipment for the manufacturing of medicine for the use of early phase clinical FDA trials. Adhering to strict standard operating procedures (SOP) and following good manufacturing practices (GMP) are required. All necessary training is provided. Successful candidates will demonstrate strong attention to detail with a safety mindset and focus within a teamwork-based work environment to ensure collective goals are achieved. No experience or education required. Individuals with a strong work ethic, mechanical aptitude, trade skills, willingness to learn and a can-do mindset are encouraged to apply. \n \nAfter an initial training period, manufacturing teams are scheduled as 4/10-hour weekday. Most shifts begin at 6:00 am.  We have a limited number of mid-shifts with a start time of 1:00pm available.\n \nAt Serán we aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a principled and positive work culture. Our operations department is expanding with a high potential for individuals to grow and build their careers. Career growth expands from Technician to Specialist I/II/III and beyond. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application!\n","description":"
    Serán BioScience is looking for dedicated individuals who are looking to learn how to become Operations Technicians and Operations Specialists. You will play an integral role in operating and maintaining specialized equipment for the manufacturing of medicine for the use of early phase clinical FDA trials. Adhering to strict standard operating procedures (SOP) and following good manufacturing practices (GMP) are required. All necessary training is provided. Successful candidates will demonstrate strong attention to detail with a safety mindset and focus within a teamwork-based work environment to ensure collective goals are achieved. No experience or education required. Individuals with a strong work ethic, mechanical aptitude, trade skills, willingness to learn and a can-do mindset are encouraged to apply.
    \n
     
    \n
    After an initial training period, manufacturing teams are scheduled as 4/10-hour weekday. Most shifts begin at 6:00 am.  We have a limited number of mid-shifts with a start time of 1:00pm available.
    \n
     
    \n
    At Serán we aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a principled and positive work culture. Our operations department is expanding with a high potential for individuals to grow and build their careers. Career growth expands from Technician to Specialist I/II/III and beyond. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application!
    ","id":"ba7fb5c4-ea51-42eb-b30e-fdcf9bf1f991","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Strictly follows standard operating procedures (SOP). 
    • \n
  • Complies with Good Manufacturing Practice (GMP). 
    • \n
  • Completes documentation, including logbooks, batch records, and quality records. 
    • \n
  • Maintains an organized, clean, and stocked production area. 
    • \n
  • Cleans tools, rooms, and equipment after use. 
    • \n
  • Weighs, measures, subdivides, and disposes of product components. 
    • \n
  • Safely handles and disposes of hazardous materials. 
    • \n
  • Operates specialized machinery to manufacture pharmaceutical products under supervision. 
    • \n
  • Works closely and communicates effectively with operations team. 
    • \n
  • Performs other related duties as assigned. 
    • \n"},{"text":"Required skills and Abilities ","content":"\n
  • Mechanical aptitude. 
    • \n
  • Strong verbal and written communication skills. 
    • \n
  • Strong organizational skills and attention to detail. 
    • \n
  • Proficient in basic math. 
    • \n
  • Strong time management skills with ability to meet deadlines. 
    • \n
  • Ability to prioritize and ask for assistance to delegate tasks when appropriate. 
    • \n
  • Ability to focus in a fast-paced environment with shifting priorities. 
    • \n
  • Proficient with Microsoft Office Suite or related software. 
    • \n"},{"text":"Education and Experience ","content":"\n
  • High School Diploma or equivalent.  
    • \n
  • Coursework or experience in chemistry or manufacturing field preferred, but not required.
    • \n
  • Operations Specialist require a minimum of 1 year of GMP experience within pharmaceutical manufacturing  
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing while monitoring equipment. 
    • \n
  • Must be able to lift up to 25 pounds regularly, and up to 55 pounds occasionally. 
    • \n
  • May require ability to work swing or weekend shift with the possibility of 12-hour shifts. 
    • \n
  • Must be able to wear a Tyvek suit with PAPR for extended periods of time. 
    • \n
  • Exposure to constant low-level equipment noise, and occasional high-level alarms. 
    • \n
  • Work near heat generating equipment. 
    • \n
  • Must be able to operate a forklift, training provided.  
    • \n
  • Move up and down ladders, kneel, squat, balance on one foot.  
    • \n
  • Move mop above head while cleaning room surfaces. 
    • \n"}],"salaryRange":{"min":26,"max":30,"currency":"USD","interval":"per-hour-wage"},"text":"Operations Technician/Specialist","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is looking for dedicated individuals who are looking to learn how to become Operations Technicians and Operations Specialists. You will play an integral role in operating and maintaining specialized equipment for the manufacturing of medicine for the use of early phase clinical FDA trials. Adhering to strict standard operating procedures (SOP) and following good manufacturing practices (GMP) are required. All necessary training is provided. Successful candidates will demonstrate strong attention to detail with a safety mindset and focus within a teamwork-based work environment to ensure collective goals are achieved. No experience or education required. Individuals with a strong work ethic, mechanical aptitude, trade skills, willingness to learn and a can-do mindset are encouraged to apply.
    \n
     
    \n
    After an initial training period, manufacturing teams are scheduled as 4/10-hour weekday. Most shifts begin at 6:00 am.  We have a limited number of mid-shifts with a start time of 1:00pm available.
    \n
     
    \n
    At Serán we aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a principled and positive work culture. Our operations department is expanding with a high potential for individuals to grow and build their careers. Career growth expands from Technician to Specialist I/II/III and beyond. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application!
    ","descriptionBodyPlain":"Serán BioScience is looking for dedicated individuals who are looking to learn how to become Operations Technicians and Operations Specialists. You will play an integral role in operating and maintaining specialized equipment for the manufacturing of medicine for the use of early phase clinical FDA trials. Adhering to strict standard operating procedures (SOP) and following good manufacturing practices (GMP) are required. All necessary training is provided. Successful candidates will demonstrate strong attention to detail with a safety mindset and focus within a teamwork-based work environment to ensure collective goals are achieved. No experience or education required. Individuals with a strong work ethic, mechanical aptitude, trade skills, willingness to learn and a can-do mindset are encouraged to apply. \n \nAfter an initial training period, manufacturing teams are scheduled as 4/10-hour weekday. Most shifts begin at 6:00 am.  We have a limited number of mid-shifts with a start time of 1:00pm available.\n \nAt Serán we aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a principled and positive work culture. Our operations department is expanding with a high potential for individuals to grow and build their careers. Career growth expands from Technician to Specialist I/II/III and beyond. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application!\n","hostedUrl":"https://jobs.lever.co/seranbio/ba7fb5c4-ea51-42eb-b30e-fdcf9bf1f991","applyUrl":"https://jobs.lever.co/seranbio/ba7fb5c4-ea51-42eb-b30e-fdcf9bf1f991/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1776716571627,"descriptionPlain":"Serán BioScience is seeking a Process Engineer to play a critical role in facility start-up, commissioning of process systems, and operational readiness for our new commercial manufacturing operations. This position will ensure that all systems, equipment, and workflows are designed, installed, and commissioned to meet cGMP standards and support efficient, compliant production. Beyond the initial launch phase, this individual will be instrumental in sustaining manufacturing operations by driving long-term operational excellence. This includes leading continuous improvement (CI) projects to ensure that all systems, equipment, and workflows remain efficient, compliant with cGMP standards, and capable of meeting evolving production demands.\n","description":"
    Serán BioScience is seeking a Process Engineer to play a critical role in facility start-up, commissioning of process systems, and operational readiness for our new commercial manufacturing operations. This position will ensure that all systems, equipment, and workflows are designed, installed, and commissioned to meet cGMP standards and support efficient, compliant production. Beyond the initial launch phase, this individual will be instrumental in sustaining manufacturing operations by driving long-term operational excellence. This includes leading continuous improvement (CI) projects to ensure that all systems, equipment, and workflows remain efficient, compliant with cGMP standards, and capable of meeting evolving production demands.
    ","id":"d6741225-7834-472e-9f5d-2e4b47374a57","lists":[{"text":"Duties and Responsibilities ","content":"
    Facility & Process System Start-Up
    \n\n
  • Lead design and engineering activities associated with process equipment for new installations and/or continuous improvements
    • \n
  • Lead engineering activities for facility process systems through design, installation, and commissioning, including CIP, purified water, solvent distribution, and compressed gases
    • \n
  • Oversee process equipment installation, commissioning, and qualification (URS, FAT, SAT, IQ/OQ/PQ)
    • \n
  • Coordinate with vendors and contractors to ensure timely and compliant start-up of manufacturing systems
    • \n
  • Develop and execute commissioning plans, risk assessments, and readiness checklists
    • \n\n
    Process Design & Optimization
    \n\n
  • Design and refine commercial-scale manufacturing processes for oral solid dosage forms and enabling technologies
    • \n
  • Perform capacity analysis, cycle time studies, and throughput modeling to ensure production efficiency
    • \n
  • Implement Lean and Six Sigma methodologies to reduce waste and improve process reliability
    • \n
  • Conduct formal risk assessments for existing process system to proactively mitigate quality and safety risks
    • \n\n
    Operational Readiness
    \n\n
  • Drive readiness activities for commercial launch, including supporting process validation and GMP documentation
    • \n
  • Partner with Validation, QA, and Manufacturing to ensure compliance with regulatory requirements
    • \n
  • Support tech transfer from development to commercial scale
    • \n
  • Collaborate with the Facilities and Maintenance teams to establish preventive and predictive maintenance schedules for process systems
    • \n
  • Draft and review standard operating procedures (SOPs) for the operation, cleaning, and troubleshooting of new process systems
    • \n\n
    Continuous Improvement
    \n\n
  • Analyze production data to identify bottlenecks and implement corrective actions
    • \n
  • Drive cost reduction initiatives and efficiency improvements without compromising quality
    • \n
  • Participate in deviation investigations and CAPA implementation
    • \n
  • Serve as the primary technical process system owner to ensure stable and robust manufacturing
    • \n\n
    Project Management
    \n\n
  • Contribute to project timelines, resource planning, and budget adherence
    • \n
  • Facilitate cross-functional project meetings and provide regular status updates to senior leadership
    • \n
  • Provide engineering input during client audits and regulatory inspections
    • \n
  • Proactively identify project risks and implement mitigation strategies 
    • \n"},{"text":"Skills, Abilities and Education Requirements ","content":"
    Required
    \n\n
  • BS/MS in Industrial Engineering, Chemical Engineering, Mechanical Engineering, or related discipline
    • \n
  • 8+ years of experience in pharmaceutical manufacturing, process engineering, or industrial engineering
    • \n
  • Hands-on experience with facility start-up, commissioning, and equipment qualification
    • \n
  • Strong knowledge of cGMP requirements and commercial manufacturing operations
    • \n
  • Proficiency in process modeling, workflow analysis, and Lean/Six Sigma tools
    • \n
  • Excellent communication and documentation skills
    • \n\n
     
    \n
    Preferred
    \n\n
  • Experience with oral solid dosage forms and enabling technologies (e.g., spray drying, blending, granulation, tableting, encapsulation, & tablet coating)
    • \n
  • Familiarity with facility design for regulated environments
    • \n
  • Knowledge of ERP/MES systems and digital manufacturing tools
    • \n
  • Project engineering experience in a regulated industry
    • \n\n
     
    \n
    Core Competencies
    \n\n
  • Analytical problem-solving and data-driven decision-making
    • \n
  • Ability to work cross-functionally in a fast-paced environment
    • \n
  • Strong organizational skills and attention to detail
    • \n
  • Continuous improvement mindset
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Prolonged periods of sitting, standing, and moving throughout a manufacturing environment
    • \n
  • Must be able to lift fifteen pounds at times
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Process Engineer","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is seeking a Process Engineer to play a critical role in facility start-up, commissioning of process systems, and operational readiness for our new commercial manufacturing operations. This position will ensure that all systems, equipment, and workflows are designed, installed, and commissioned to meet cGMP standards and support efficient, compliant production. Beyond the initial launch phase, this individual will be instrumental in sustaining manufacturing operations by driving long-term operational excellence. This includes leading continuous improvement (CI) projects to ensure that all systems, equipment, and workflows remain efficient, compliant with cGMP standards, and capable of meeting evolving production demands.
    ","descriptionBodyPlain":"Serán BioScience is seeking a Process Engineer to play a critical role in facility start-up, commissioning of process systems, and operational readiness for our new commercial manufacturing operations. This position will ensure that all systems, equipment, and workflows are designed, installed, and commissioned to meet cGMP standards and support efficient, compliant production. Beyond the initial launch phase, this individual will be instrumental in sustaining manufacturing operations by driving long-term operational excellence. This includes leading continuous improvement (CI) projects to ensure that all systems, equipment, and workflows remain efficient, compliant with cGMP standards, and capable of meeting evolving production demands.\n","hostedUrl":"https://jobs.lever.co/seranbio/d6741225-7834-472e-9f5d-2e4b47374a57","applyUrl":"https://jobs.lever.co/seranbio/d6741225-7834-472e-9f5d-2e4b47374a57/apply"},{"additionalPlain":"","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Project Management","allLocations":["Bend, Oregon"]},"createdAt":1774052303604,"descriptionPlain":"","description":"
    The Project Manager role with Seran Bioscience plays a crucial role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines, influencing, and supporting the internal teams, and for reporting regular updates directly to clients. Each project lifespan can be broken into 6 unique phases for which the project manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. 
    ","id":"ab556895-adf4-4ae8-aadb-20412cfef9d9","lists":[{"text":"Duties and Responsibilities ","content":"
    \n
    \n
    \n
    "},{"text":"Required Skills and Abilities","content":"
    \n
    \n
    \n
    "},{"text":"Education and Experience ","content":"
    \n
    "},{"text":"Physical Requirements ","content":"
    \n
    "}],"text":"Project Manager","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    The Project Manager role with Seran Bioscience plays a crucial role in the CMO lifespan of a drug. With this role, you work closely with clients to manage a project from initiation, through formulation and development, manufacturing, and beyond completion. You will need excellent collaboration, communication, management, organization, and planning abilities. You will be responsible for managing project timelines, influencing, and supporting the internal teams, and for reporting regular updates directly to clients. Each project lifespan can be broken into 6 unique phases for which the project manager is responsible: Initiation, Planning, Execution, Coordination, Monitoring, and Closing. 
    ","descriptionBodyPlain":"","hostedUrl":"https://jobs.lever.co/seranbio/ab556895-adf4-4ae8-aadb-20412cfef9d9","applyUrl":"https://jobs.lever.co/seranbio/ab556895-adf4-4ae8-aadb-20412cfef9d9/apply"},{"additional":"","additionalPlain":"","categories":{"commitment":"Full-time Non-exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Control","allLocations":["Bend, Oregon"]},"createdAt":1776274448683,"descriptionPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department seeks a Laboratory Technician to play a critical role in supporting the ongoing sample testing performed by the Quality Control lab in support of good manufacturing practices (GMP) and customer satisfaction. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply.   \n","description":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department seeks a Laboratory Technician to play a critical role in supporting the ongoing sample testing performed by the Quality Control lab in support of good manufacturing practices (GMP) and customer satisfaction. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply.   
    ","id":"15088143-0817-45c3-ac36-71944c732f78","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Conducts appearance testing, solution preparation and pH measurements
    • \n
  • Supports raw materials sampling
    • \n
  • Logs-in samples and standards
    • \n
  • Perform routine equipment, laboratory, and instrument maintenance 
    • \n
  • Clean lab glassware and disposes of solvent
    • \n"},{"text":"Required Knowledge, Skills, and Abilities ","content":"\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent interpersonal and internal customer service skills 
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Ability to work as a team
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n"},{"text":"Education and Experience ","content":"\n
  • High school diploma with laboratory experience
    • \n
  • Bachelor’s degree or coursework in chemical engineering, chemistry, materials science, or related field preferred
    • \n
  • Those with limited lab experience are still encouraged to apply
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting at a desk and working on a computer 
    • \n
  • Must be able to lift up to 15 pounds regularly, and up to 30 pounds occasionally 
    • \n"}],"text":"QC Lab Technician","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department seeks a Laboratory Technician to play a critical role in supporting the ongoing sample testing performed by the Quality Control lab in support of good manufacturing practices (GMP) and customer satisfaction. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply.   
    ","descriptionBodyPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department seeks a Laboratory Technician to play a critical role in supporting the ongoing sample testing performed by the Quality Control lab in support of good manufacturing practices (GMP) and customer satisfaction. This role requires strong attention to detail and focus within a fast-paced work environment. Successful candidates will demonstrate strengths in teamwork, self-discipline, and proactive communication to ensure collective goals are achieved. Those with limited lab experience are still encouraged to apply.   \n","hostedUrl":"https://jobs.lever.co/seranbio/15088143-0817-45c3-ac36-71944c732f78","applyUrl":"https://jobs.lever.co/seranbio/15088143-0817-45c3-ac36-71944c732f78/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Assurance","allLocations":["Bend, Oregon"]},"createdAt":1779487652644,"descriptionPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","description":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing and testing pharmaceutical products. Tasks include auditing and audit support, supplier quality management, and continuous improvement.  Additional responsibilities include Quality Management System, risk analyses, change management and investigations/CAPA. Preference will be given to candidates with Quality Assurance experience in the pharmaceutical industry, while those with Quality oversight experience are encouraged to apply.
    ","id":"5c499d60-3da6-4908-8436-84fc95abd4c0","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Participates in internal and third-party audits.
    • \n
  • Supports client audits and regulatory inspections
    • \n
  • Supports company’s supplier quality program
    • \n
  • Assists in the oversight and implementation of continuous improvement of the company’s Quality systems 
    • \n
  • Supports the risk management program and conducts risk assessments
    • \n
  • Document authorship, review, and approval of SOPs, reports, and quality records.
    • \n
  • Other related duties as assigned 
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Knowledge of GMP and FDA regulations for drug manufacturing (21CFR 210-211)
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n"},{"text":"Education and Experience ","content":"\n
  • Minimum of a Bachelor's Degree, preferably in a scientific discipline 
    • \n
  • 3+ years previous manufacturing, quality control, or quality assurance experience 
    • \n
  • Working knowledge of Veeva preferred
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Quality Assurance Associate II/III","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing and testing pharmaceutical products. Tasks include auditing and audit support, supplier quality management, and continuous improvement.  Additional responsibilities include Quality Management System, risk analyses, change management and investigations/CAPA. Preference will be given to candidates with Quality Assurance experience in the pharmaceutical industry, while those with Quality oversight experience are encouraged to apply.
    ","descriptionBodyPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","hostedUrl":"https://jobs.lever.co/seranbio/5c499d60-3da6-4908-8436-84fc95abd4c0","applyUrl":"https://jobs.lever.co/seranbio/5c499d60-3da6-4908-8436-84fc95abd4c0/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Assurance","allLocations":["Bend, Oregon"]},"createdAt":1779488262621,"descriptionPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","description":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to support quality systems programs. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department in a GMP facility manufacturing pharmaceutical products. Tasks include supporting quality system programs such as document management, training, and quality event programs.  Additional responsibilities include assisting in the maintenance of the electronic Quality Management System, conducting risk analyses and investigations, and participating in audits and inspections. Preference will be given to candidates within the pharmaceutical industry, while those with Quality oversight experience encouraged to apply.
    ","id":"4c5831b0-eea0-4ab4-a129-be3e3dff9b56","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Supports the implementation and continuous improvement of the company’s Quality systems 
    • \n
  • Assists in monitoring of Serán quality systems through trending and metrics analysis
    • \n
  • Supports the management of Serán’s quality systems through program oversight and eQMS administrative functions.
    • \n
  • Document authorship, review, and approval of SOPs, reports, and quality records
    • \n
  • Oversight of investigation and CAPA program management 
    • \n
  • Supports internal audits, client audits and regulatory inspections, as needed
    • \n
  • Other related duties as assigned 
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Knowledge of GMP and FDA regulations for clinical trial materials preferred
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Demonstrated experience in characterization and analytical techniques relevant to the pharmaceutical industry
    • \n
  • Demonstrated experience with advanced laboratory and data analysis skills preferred
    • \n
  • Strong analytical and problem-solving skills
    • \n"},{"text":"Education and Experience ","content":"\n
  • Minimum of a Bachelor's Degree, preferably in a scientific discipline 
    • \n
  • 3+ years previous manufacturing, quality control, or quality assurance experience 
    • \n
  • Working knowledge of Veeva and/or SAP preferred
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Quality Assurance Associate II/III -Quality Management System","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to support quality systems programs. As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department in a GMP facility manufacturing pharmaceutical products. Tasks include supporting quality system programs such as document management, training, and quality event programs.  Additional responsibilities include assisting in the maintenance of the electronic Quality Management System, conducting risk analyses and investigations, and participating in audits and inspections. Preference will be given to candidates within the pharmaceutical industry, while those with Quality oversight experience encouraged to apply.
    ","descriptionBodyPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","hostedUrl":"https://jobs.lever.co/seranbio/4c5831b0-eea0-4ab4-a129-be3e3dff9b56","applyUrl":"https://jobs.lever.co/seranbio/4c5831b0-eea0-4ab4-a129-be3e3dff9b56/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Assurance","allLocations":["Bend, Oregon"]},"createdAt":1778874908621,"descriptionPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","description":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. 
    \n
     
    \n
    This role will support the alternative manufacturing schedule from Monday - Thursday, beginning at 2:00 pm and ending at 1:00 am. Experience specific to Serán's manufacturing capabilities and confidence to make independent decisions in alignment with Company policies and risk mitigation philosophies will be critical to this role.  
    \n
     
    \n
     
    ","id":"d8351dac-0a2c-4961-be4d-a2eab23aa58f","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
    • \n
  • Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas
    • \n
  • Initiates and oversees investigations
    • \n
  • Manages corrective and preventive actions (CAPA)
    • \n
  • Supports internal audits, client audits and regulatory inspections, with the potential to host 
    • \n
  • Manages controlled document issuance and archival
    • \n
  • Performs quality reviews with minimal oversight 
    • \n
  • Communicates quality-related information to internal teams with minimal guidance
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n
  • Performs all other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required
    • \n
  • Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrates the ability to collaborate and work in cross-functional teams
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n
  • Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree, preferably in a scientific discipline
    • \n
  • 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II
    • \n
  • 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III
    • \n
  • Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Quality Assurance Associate II/III (Swing Shift)","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. 
    \n
     
    \n
    This role will support the alternative manufacturing schedule from Monday - Thursday, beginning at 2:00 pm and ending at 1:00 am. Experience specific to Serán's manufacturing capabilities and confidence to make independent decisions in alignment with Company policies and risk mitigation philosophies will be critical to this role.  
    \n
     
    \n
     
    ","descriptionBodyPlain":"Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán’s Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience. \n\nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.\n","hostedUrl":"https://jobs.lever.co/seranbio/d8351dac-0a2c-4961-be4d-a2eab23aa58f","applyUrl":"https://jobs.lever.co/seranbio/d8351dac-0a2c-4961-be4d-a2eab23aa58f/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nLevel and compensation will be based on experience. \n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Level and compensation will be based on experience.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1774385707732,"descriptionPlain":"Serán BioScience is expanding and looking for a Quality Assurance Engineer with industry experience to join at this exciting time. The QA Engineer will be part of a cross functional team that will be responsible for the review and/or approval of qualification/validation of all the lifecycle activities associated with facilities, utilities, equipment, process, cleaning, and computerized systems. The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway. \n \nThe development and execution of these deliverables requires direct communication with internal and external cross functional teams. Successful candidates will understand that effective communication is essential for alignment on strategies and approaches, and correcting deficiencies while maintaining good working relationships. Qualified candidates will have a thorough understanding of current regulations and guidelines such as but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5 is required. \n","description":"
    Serán BioScience is expanding and looking for a Quality Assurance Engineer with industry experience to join at this exciting time. The QA Engineer will be part of a cross functional team that will be responsible for the review and/or approval of qualification/validation of all the lifecycle activities associated with facilities, utilities, equipment, process, cleaning, and computerized systems. The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway.
    \n
     
    \n
    The development and execution of these deliverables requires direct communication with internal and external cross functional teams. Successful candidates will understand that effective communication is essential for alignment on strategies and approaches, and correcting deficiencies while maintaining good working relationships. Qualified candidates will have a thorough understanding of current regulations and guidelines such as but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5 is required.
    ","id":"0c9e7d62-9977-4058-92f8-4ae7caebc38a","lists":[{"text":"Duties and Responsibilities","content":"\n
  • Generates and/or supports the generation of risk assessments, user requirements specifications (URS), C&Q plans, change controls, SOPs, CAPAs, and other relevant documents
    • \n
  • Supports validation lifecycle activities such as, but not limited to, change management, periodic reviews, and re-qualification to ensure that qualified systems remain in their validated state
    • \n
  • Makes compliance decisions to support commercial operations
    • \n
  • Mentors colleagues on the reasons or justifications of the requirements and practices
    • \n
  • Drives process improvement initiatives
    • \n
  • Provides support during clients and regulatory audits
    • \n
  • Performs other related duties as assigned
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Understanding of current regulations and guidelines (e.g., 21 CFR Parts 11, 210, and 211, EudraLex Volume 4 - Annex 15, GAMP 5, etc.) and how to apply them to support the validation effort
    • \n
  • Technical writing skills to effectively develop procedures, discrepancies, change controls, CAPAs and associated documents needed to support the validation effort
    • \n
  • Hands-on experience with the qualification of facilities, utilities, equipment and/or computerized systems, cleaning or process validation (Experience in at least two of these areas is required)
    • \n
  • Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team
    • \n
  • Strong time-management skills and the ability to organize and coordinate multiple projects at a time
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
    • \n
  • Ability to prioritize tasks and to keep leadership apprised of performance to timelines
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Experience in Oral Solid Dose operations and spray drying is preferable
    • \n
  • Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with aptitude to learn new software and systems
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree in a science, engineering, or related field
    • \n
  • Minimum of 4 years required within pharmaceutical industry, with preference given to those with 5-10 years of experience
    • \n
  • Minimum of 4 years of experience performing qualifications and/or validations is required 
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods sitting at a desk and working on a computer
    • \n
  • Prolonged periods of mobility between offices and campus buildings
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Quality Assurance Engineer","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is expanding and looking for a Quality Assurance Engineer with industry experience to join at this exciting time. The QA Engineer will be part of a cross functional team that will be responsible for the review and/or approval of qualification/validation of all the lifecycle activities associated with facilities, utilities, equipment, process, cleaning, and computerized systems. The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway.
    \n
     
    \n
    The development and execution of these deliverables requires direct communication with internal and external cross functional teams. Successful candidates will understand that effective communication is essential for alignment on strategies and approaches, and correcting deficiencies while maintaining good working relationships. Qualified candidates will have a thorough understanding of current regulations and guidelines such as but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5 is required.
    ","descriptionBodyPlain":"Serán BioScience is expanding and looking for a Quality Assurance Engineer with industry experience to join at this exciting time. The QA Engineer will be part of a cross functional team that will be responsible for the review and/or approval of qualification/validation of all the lifecycle activities associated with facilities, utilities, equipment, process, cleaning, and computerized systems. The focus of this position will be to support the Commercial Manufacturing Facility that is currently underway. \n \nThe development and execution of these deliverables requires direct communication with internal and external cross functional teams. Successful candidates will understand that effective communication is essential for alignment on strategies and approaches, and correcting deficiencies while maintaining good working relationships. Qualified candidates will have a thorough understanding of current regulations and guidelines such as but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5 is required. \n","hostedUrl":"https://jobs.lever.co/seranbio/0c9e7d62-9977-4058-92f8-4ae7caebc38a","applyUrl":"https://jobs.lever.co/seranbio/0c9e7d62-9977-4058-92f8-4ae7caebc38a/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Control","allLocations":["Bend, Oregon"]},"createdAt":1778255595887,"descriptionPlain":"Serán BioScience is searching for a Sample Associate to help organize and coordinate inventory for the Quality Control testing laboratory. The Sample Associate plays a key role supporting sample coordination by managing QC sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing.  This role combines organizational support to a laboratory environment and is a great opportunity for entry-level professional laboratory experience.  Preference will be given to those who have strong attention to detail with firm understanding of documentation compliance and record keeping.  Those who have a strong desire to support laboratory research and development encouraged to apply.\n \nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.  \n","description":"
    Serán BioScience is searching for a Sample Associate to help organize and coordinate inventory for the Quality Control testing laboratory. The Sample Associate plays a key role supporting sample coordination by managing QC sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing.  This role combines organizational support to a laboratory environment and is a great opportunity for entry-level professional laboratory experience.  Preference will be given to those who have strong attention to detail with firm understanding of documentation compliance and record keeping.  Those who have a strong desire to support laboratory research and development encouraged to apply.
    \n
     
    \n
    Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.  
    ","id":"065ec945-1975-421b-a912-17775eae7190","lists":[{"text":"Duties and Responsibilities ","content":"
    \n\n
  • Sample coordination and receipt from other departments for internal and external testing
    • \n
  • Manages QC sample inventory, including in-process, release, retain, and stability samples
    • \n
  • Ships samples to external Contract Testing Laboratories (CTL)
    • \n
  • Follows up with CTLs on testing and turnaround times to ensure testing deadlines are met
    • \n
  • Performs data entry for tracking & trending of sample management and laboratory reports
    • \n
  • Keeps accurate and complete records per cGMP.
    • \n
  • Effectively communicates updates and results from CTLs to internal team and management
    • \n
  • Initiates laboratory investigations, including OOS
    • \n
  • All other duties as assigned
    • \n\n
    "},{"text":"Required Skills and Abilities ","content":"
    \n\n
  • Strong verbal and written communication skills
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Strong organizational skills and attention to detail
    • \n
  • Strong time management skills with a proven ability to meet deadlines
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Ability to prioritize tasks and to keep leadership apprised of performance to timelines
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Proficient with Microsoft Office Suite or related software
    • \n\n
    "},{"text":"Education and Experience ","content":"
    \n\n
  • High School diploma
    • \n
  • 1-2 years experience in a position requiring strong analytical skills (measurements, math, labeling, working with spreadsheets)
    • \n\n
    "},{"text":"Physical Requirements ","content":"
    \n\n
  • Prolonged periods of sitting at a desk and working on a computer
    • \n
  • Prolonged periods of sitting or standing in laboratory environment
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n\n
    "}],"text":"Quality Control Sample Associate","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for a Sample Associate to help organize and coordinate inventory for the Quality Control testing laboratory. The Sample Associate plays a key role supporting sample coordination by managing QC sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing.  This role combines organizational support to a laboratory environment and is a great opportunity for entry-level professional laboratory experience.  Preference will be given to those who have strong attention to detail with firm understanding of documentation compliance and record keeping.  Those who have a strong desire to support laboratory research and development encouraged to apply.
    \n
     
    \n
    Serán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.  
    ","descriptionBodyPlain":"Serán BioScience is searching for a Sample Associate to help organize and coordinate inventory for the Quality Control testing laboratory. The Sample Associate plays a key role supporting sample coordination by managing QC sample inventory, including the receipt, handling, shipment, and storage of samples supporting the GMP retention program, stability program, and external Contract Testing Laboratories (CTL) testing.  This role combines organizational support to a laboratory environment and is a great opportunity for entry-level professional laboratory experience.  Preference will be given to those who have strong attention to detail with firm understanding of documentation compliance and record keeping.  Those who have a strong desire to support laboratory research and development encouraged to apply.\n \nSerán BioScience develops and manufactures novel drug products for a variety of pharmaceutical applications. We aim to build a workforce that is collaborative, creative, and kind. In addition to the skills required of the role, qualified candidates will approach their work with integrity and enthusiasm to promote a positive work culture. Employees are awarded generous PTO accrual, low-cost health benefits, and a 5% 401(k) contribution that does not require an employee match or vesting. Want to learn more about what we do, who we are, and how you can contribute? We look forward to seeing your application.  \n","hostedUrl":"https://jobs.lever.co/seranbio/065ec945-1975-421b-a912-17775eae7190","applyUrl":"https://jobs.lever.co/seranbio/065ec945-1975-421b-a912-17775eae7190/apply"},{"additionalPlain":"Benefits\n \nVisit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n

    Benefits

    \n
     
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Non-exempt","department":"Quality","location":"Bend, Oregon","team":"Quality Control","allLocations":["Bend, Oregon"]},"createdAt":1778630302119,"descriptionPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department is seeking a Quality Control Scientist level I or II who performs and supports sample testing activities in the Quality Control laboratory, upholding GMP practices and timely completion of client deliverables.\n","description":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department is seeking a Quality Control Scientist level I or II who performs and supports sample testing activities in the Quality Control laboratory, upholding GMP practices and timely completion of client deliverables.
    ","id":"0f8fb69b-cf1f-4d27-b3da-a1b4fc4625a6","lists":[{"text":"Duties and Responsibilities","content":"
    \n\n
  • Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies.
    • \n
  • Performs routine extractions for dissolution, assay, and impurities testing.
    • \n
  • Performs routine testing using analytical equipment including but not limited to KFC, dissolution apparatus, water activity, FTIR, etc.
    • \n
  • Conducts appearance testing, raw materials sampling, solution preparation, and pH measurements.
    • \n
  • Drafts stability tables, sets-up stability studies, logs-in samples and standards.
    • \n
  • Cleans lab and glassware and disposes of analytical waste appropriately.
    • \n
  • Participates in process improvement and other non-routine projects.
    • \n
  • Conducts peer review of routine testing at the discretion of management.
    • \n
  • Performs hypothesis testing or investigative work for OOS results under management and SME guidance.
    • \n
  • Trains and mentors staff on established processes and procedures.
    • \n
  • Demonstrates cross-functional support capabilities with other QC teams.
    • \n
  • Adheres to consistent and predictable in-person attendance.
    • \n
  • Responsibilities may increase in scope to align with company initiatives.
    • \n\n
    "},{"text":"Required Skills and Abilities","content":""},{"text":"Education and Experience","content":"
    \n
    All levels: Bachelor’s degree in a scientific discipline or related field.
    \n
     
    \n
     
    \n
    For a level I applicant, we are seeking 2 years of dedicated lab experience in addition to the science education. GMP setting experience not required but preferable.
    \n
     
    \n
    For a level II applicant, we are seeking 3 years of dedicated lab experience (including 2 years in a GMP setting) in addition to the science education.
    \n
    "}],"text":"Quality Control Scientist I or II","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department is seeking a Quality Control Scientist level I or II who performs and supports sample testing activities in the Quality Control laboratory, upholding GMP practices and timely completion of client deliverables.
    ","descriptionBodyPlain":"Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. Our Quality Control Department is seeking a Quality Control Scientist level I or II who performs and supports sample testing activities in the Quality Control laboratory, upholding GMP practices and timely completion of client deliverables.\n","hostedUrl":"https://jobs.lever.co/seranbio/0f8fb69b-cf1f-4d27-b3da-a1b4fc4625a6","applyUrl":"https://jobs.lever.co/seranbio/0f8fb69b-cf1f-4d27-b3da-a1b4fc4625a6/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Process and Product Development","location":"Bend, Oregon","team":"Process and Product Development","allLocations":["Bend, Oregon"]},"createdAt":1777067116132,"descriptionPlain":"Serán is seeking a Scientist I supporting Product Development  who will support the formulation and design of pharmaceutical drug under the guidance of senior team members. A typical project requires defining the drug delivery and product design challenges, developing prototypes that address the challenges, and evaluating prototype performance. The successful candidate will pair a strong fundamental understanding of physical chemistry and material science with aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. The Scientist will collaborate with experts in process development and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","description":"
    \n

    Serán is seeking a Scientist I supporting Product Development  who will support the formulation and design of pharmaceutical drug under the guidance of senior team members. A typical project requires defining the drug delivery and product design challenges, developing prototypes that address the challenges, and evaluating prototype performance. The successful candidate will pair a strong fundamental understanding of physical chemistry and material science with aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. The Scientist will collaborate with experts in process development and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.

    \n
    ","id":"4d5cb5aa-e33c-480b-9db1-3707b321d84a","lists":[{"text":"Duties and Responsibilities","content":"\n
  • Follows written protocols to execute basic and advanced procedures such as analytical protocols, laboratory experiments, or manufacturing processes
    • \n
  • Develops experimental protocols and templates with guidance
    • \n
  • Identifies out of trend data and proposes hypothesis and next steps with guidance
    • \n
  • Summarizes, reports, and analyzes data to draw conclusions with guidance
    • \n
  • Contributes to laboratory, instrument, and/or equipment maintenance and coordination
    • \n
  • Communicates technical information to internal team
    • \n
  • Communicates technical information to external partners with guidance
    • \n
  • Participates as technical lead in project teams with guidance
    • \n
  • Contributes to technical reports and presentations with guidance
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n\n
     
    "},{"text":"Required Skills and Abilities","content":"
    \n\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Ability to work collaboratively in a cross-functional team environment
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Experience with basic laboratory skills
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Accepts and addresses feedback from a variety of sources and constructively manages conflict
    • \n\n
    "},{"text":"Education and Experience","content":"
    \n\n
  • B.S. or higher in Science or Engineering discipline
    • \n\n
    "},{"text":"","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 25 pounds regularly and up to 50 pounds occasionally
    • \n
  • Motor skills required for basic laboratory operations (pouring liquids, using utensils to transfer powders, visual assessments)
    • \n\n
    "}],"text":"Scientist I","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    \n

    Serán is seeking a Scientist I supporting Product Development  who will support the formulation and design of pharmaceutical drug under the guidance of senior team members. A typical project requires defining the drug delivery and product design challenges, developing prototypes that address the challenges, and evaluating prototype performance. The successful candidate will pair a strong fundamental understanding of physical chemistry and material science with aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. The Scientist will collaborate with experts in process development and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.

    \n
    ","descriptionBodyPlain":"Serán is seeking a Scientist I supporting Product Development  who will support the formulation and design of pharmaceutical drug under the guidance of senior team members. A typical project requires defining the drug delivery and product design challenges, developing prototypes that address the challenges, and evaluating prototype performance. The successful candidate will pair a strong fundamental understanding of physical chemistry and material science with aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. The Scientist will collaborate with experts in process development and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","hostedUrl":"https://jobs.lever.co/seranbio/4d5cb5aa-e33c-480b-9db1-3707b321d84a","applyUrl":"https://jobs.lever.co/seranbio/4d5cb5aa-e33c-480b-9db1-3707b321d84a/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Information Technology","location":"Bend, Oregon","team":"IT","allLocations":["Bend, Oregon"]},"createdAt":1778541682460,"descriptionPlain":"Serán is seeking a Senior Automation Engineer to manage automated manufacturing and process equipment needs, control systems, and support facility design and qualifications as part of the Seran’s expansion efforts.  This position will require a strong engineering background in qualified pharmaceutical/biotech industrial practices, preferably with specialized expertise in spray drying and solid dosage form applications and technology. Primary duties include design of automated equipment and machinery used to complete otherwise manual processes and tasks, evaluation and testing of existing automated systems, defining areas where introducing automation could improve production and efficiency, and providing technical support in relation to automated systems when necessary.\n","description":"
    Serán is seeking a Senior Automation Engineer to manage automated manufacturing and process equipment needs, control systems, and support facility design and qualifications as part of the Seran’s expansion efforts.  This position will require a strong engineering background in qualified pharmaceutical/biotech industrial practices, preferably with specialized expertise in spray drying and solid dosage form applications and technology. Primary duties include design of automated equipment and machinery used to complete otherwise manual processes and tasks, evaluation and testing of existing automated systems, defining areas where introducing automation could improve production and efficiency, and providing technical support in relation to automated systems when necessary.
    ","id":"828d424a-95d7-400d-8a4b-3ce2f527b211","lists":[{"text":"Duties and Responsibilities","content":"
    \n
    "},{"text":"Required Skills and Abilities","content":"
    \n
    "},{"text":"Education and Experience","content":"
    \n
    "},{"text":"Physical Requirements","content":"
    \n
    "}],"text":"Senior Automation Engineer","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán is seeking a Senior Automation Engineer to manage automated manufacturing and process equipment needs, control systems, and support facility design and qualifications as part of the Seran’s expansion efforts.  This position will require a strong engineering background in qualified pharmaceutical/biotech industrial practices, preferably with specialized expertise in spray drying and solid dosage form applications and technology. Primary duties include design of automated equipment and machinery used to complete otherwise manual processes and tasks, evaluation and testing of existing automated systems, defining areas where introducing automation could improve production and efficiency, and providing technical support in relation to automated systems when necessary.
    ","descriptionBodyPlain":"Serán is seeking a Senior Automation Engineer to manage automated manufacturing and process equipment needs, control systems, and support facility design and qualifications as part of the Seran’s expansion efforts.  This position will require a strong engineering background in qualified pharmaceutical/biotech industrial practices, preferably with specialized expertise in spray drying and solid dosage form applications and technology. Primary duties include design of automated equipment and machinery used to complete otherwise manual processes and tasks, evaluation and testing of existing automated systems, defining areas where introducing automation could improve production and efficiency, and providing technical support in relation to automated systems when necessary.\n","hostedUrl":"https://jobs.lever.co/seranbio/828d424a-95d7-400d-8a4b-3ce2f527b211","applyUrl":"https://jobs.lever.co/seranbio/828d424a-95d7-400d-8a4b-3ce2f527b211/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Process and Product Development","location":"Bend, Oregon","team":"Process and Product Development","allLocations":["Bend, Oregon"]},"createdAt":1777065106355,"descriptionPlain":"Serán is seeking a Senior Engineer to join their Process Development team who will support process development of pharmaceutical drug products from early clinical manufactures through late-stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. A clear communication style and emerging aptitude for strategic thinking will allow the Senior Engineer to navigate important decisions with project sponsors. The Senior Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","description":"
    Serán is seeking a Senior Engineer to join their Process Development team who will support process development of pharmaceutical drug products from early clinical manufactures through late-stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. A clear communication style and emerging aptitude for strategic thinking will allow the Senior Engineer to navigate important decisions with project sponsors. The Senior Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.
    ","id":"fa756afc-10a4-4ffc-a511-9e0796dbad7a","lists":[{"text":"Supervisory Responsibilities","content":"
    \n\n
  • May oversee part of the daily workflow of the department
    • \n
  • May provide constructive and timely performance evaluations
    • \n
  • May coordinate the work of other team members
    • \n
  • May provide technical guidance and direction
    • \n
  • May provide mentorship
    • \n\n
    "},{"text":"Duties/Responsibilities","content":"
    \n\n
  • Independently develops experimental protocols and templates based on project need
    • \n
  • Independently summarizes, reports, and analyzes data to draw conclusions and proposes next steps
    • \n
  • Identifies out of trend data, forms hypothesis and investigates
    • \n
  • Evaluates data and draws conclusions across data sets/projects
    • \n
  • Contributes to laboratory, instrument, and/or equipment maintenance and coordination
    • \n
  • Communicates technical information to internal team
    • \n
  • Independently communicates technical information to external partners
    • \n
  • Independently leads projects
    • \n
  • Authors technical reports and presentations with minimal guidance
    • \n
  • Develops and manages workplans
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n\n
    "},{"text":"Requires Skills/Abilities","content":"
    \n\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Demonstrated experience in pharmaceutical product and / or process development
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Demonstrated experience with advanced laboratory and data analysis skills
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n\n
    "},{"text":"Education and Experience","content":"
    \n\n
  • B.S. in Science or Engineering discipline with 5+ years of experience,
    • \n
  • M.S. in Science or Engineering discipline with 3+ years of experience, or
    • \n
  • PhD in Science or Engineering discipline, with preference given to candidates with relevant industrial experience
    • \n\n
    "},{"text":"Physical Requirements","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 25 pounds regularly and up to 50 pounds occasionally
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n\nMotor skills required for basic laboratory operations (pouring liquids, using utensils to transfer powders, visual assessments)
    "}],"text":"Senior Engineer, Process Development","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán is seeking a Senior Engineer to join their Process Development team who will support process development of pharmaceutical drug products from early clinical manufactures through late-stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. A clear communication style and emerging aptitude for strategic thinking will allow the Senior Engineer to navigate important decisions with project sponsors. The Senior Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.
    ","descriptionBodyPlain":"Serán is seeking a Senior Engineer to join their Process Development team who will support process development of pharmaceutical drug products from early clinical manufactures through late-stage process validation. This position will require aptitude for hands-on execution, hypothesis-driven experimental design, and data analysis. A clear communication style and emerging aptitude for strategic thinking will allow the Senior Engineer to navigate important decisions with project sponsors. The Senior Engineer will collaborate with experts in formulation and product design and analytical sciences to form a comprehensive, multi-disciplinary project team that consistently meets milestones and objectives.\n","hostedUrl":"https://jobs.lever.co/seranbio/fa756afc-10a4-4ffc-a511-9e0796dbad7a","applyUrl":"https://jobs.lever.co/seranbio/fa756afc-10a4-4ffc-a511-9e0796dbad7a/apply"},{"additionalPlain":"Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Compensation correlates to skills and experience presented by selected candidate. Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1774304076051,"descriptionPlain":"Serán is seeking a hands-on Process Engineer with deep spray drying expertise to develop, scale, and transfer robust processes for small molecule and complex drug products. You will lead end-to-end unit operations—from feasibility and DOE through clinical/commercial scale-up—while ensuring safety, quality (GMP), and operational excellence in a fast-paced, collaborative environment.\n \nAs the system owner, the Process Engineer oversees creation and revision of equipment documentation packages, supports regulatory and client audits, and ensures alignment with cGMP expectations. They maintain a deep, data‑driven understanding of equipment performance, analyze trends to anticipate issues, and drive improvements that enhance reliability, yield, and product quality. The role collaborates closely with Maintenance, Quality, Validation, and Manufacturing to coordinate spare‑parts strategies, preventative maintenance, calibration schedules, and implementation of clean‑in‑place systems. In a CDMO setting, the engineer also partners with clients and internal teams to support tech transfers, scale‑up activities, and lifecycle management of spray‑drying processes.\n","description":"
    Serán is seeking a hands-on Process Engineer with deep spray drying expertise to develop, scale, and transfer robust processes for small molecule and complex drug products. You will lead end-to-end unit operations—from feasibility and DOE through clinical/commercial scale-up—while ensuring safety, quality (GMP), and operational excellence in a fast-paced, collaborative environment.
    \n
     
    \n
    As the system owner, the Process Engineer oversees creation and revision of equipment documentation packages, supports regulatory and client audits, and ensures alignment with cGMP expectations. They maintain a deep, data‑driven understanding of equipment performance, analyze trends to anticipate issues, and drive improvements that enhance reliability, yield, and product quality. The role collaborates closely with Maintenance, Quality, Validation, and Manufacturing to coordinate spare‑parts strategies, preventative maintenance, calibration schedules, and implementation of clean‑in‑place systems. In a CDMO setting, the engineer also partners with clients and internal teams to support tech transfers, scale‑up activities, and lifecycle management of spray‑drying processes.
    ","id":"afe675bc-c9b1-4d19-911d-1a2280e61ed7","lists":[{"text":"Duties and Responsibilities ","content":"
    \n\n
  • System owner of commercial spray drying equipment, including solution preparation, spray drying, and secondary drying systems
    • \n
  • Oversee creation of and revisions of equipment documentation packages
    • \n\n
    "},{"text":"Required Skills and Abilities ","content":"
    \n\n
  • Expertise with common unit operations for spray drying, including solution preparation and secondary drying
    • \n
  • Demonstrated experience working in and supporting GMP manufacturing lines
    • \n
  • Demonstrated experience with principles of risk-based decision making and common tools for risk analysis
    • \n
  • Ability to apply rigorous scientific and engineering principles to guide practical decisions
    • \n
  • Working knowledge of process thermodynamics, fluid mechanics, and heat and mass transfer
    • \n
  • Ability to analyze complex data sets
    • \n
  • Excellent verbal and written communication skills
    • \n
  • Ability to collaborate effectively with stakeholders across the organization
    • \n
  • Excellent time management skills, with an ability to prioritize and / or delegate tasks appropriately to meet deadlines
    • \n
  • Ability to function in a fast-paced team environment
    • \n\n
    "},{"text":"Education and Experience ","content":""},{"text":"Physical Requirements ","content":"\n
  • Work in lab/pilot-plant setting with solvents and fine powders; PPE required.
    • \n
  • Ability to lift up to ~25–40 lbs occasionally; extended periods of standing during operations.
    • \n
  • Some travel may be required for vendor FAT/SAT or client tech transfer (≤10%).
    • \n"}],"text":"Senior Process Engineer, Spray Drying","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán is seeking a hands-on Process Engineer with deep spray drying expertise to develop, scale, and transfer robust processes for small molecule and complex drug products. You will lead end-to-end unit operations—from feasibility and DOE through clinical/commercial scale-up—while ensuring safety, quality (GMP), and operational excellence in a fast-paced, collaborative environment.
    \n
     
    \n
    As the system owner, the Process Engineer oversees creation and revision of equipment documentation packages, supports regulatory and client audits, and ensures alignment with cGMP expectations. They maintain a deep, data‑driven understanding of equipment performance, analyze trends to anticipate issues, and drive improvements that enhance reliability, yield, and product quality. The role collaborates closely with Maintenance, Quality, Validation, and Manufacturing to coordinate spare‑parts strategies, preventative maintenance, calibration schedules, and implementation of clean‑in‑place systems. In a CDMO setting, the engineer also partners with clients and internal teams to support tech transfers, scale‑up activities, and lifecycle management of spray‑drying processes.
    ","descriptionBodyPlain":"Serán is seeking a hands-on Process Engineer with deep spray drying expertise to develop, scale, and transfer robust processes for small molecule and complex drug products. You will lead end-to-end unit operations—from feasibility and DOE through clinical/commercial scale-up—while ensuring safety, quality (GMP), and operational excellence in a fast-paced, collaborative environment.\n \nAs the system owner, the Process Engineer oversees creation and revision of equipment documentation packages, supports regulatory and client audits, and ensures alignment with cGMP expectations. They maintain a deep, data‑driven understanding of equipment performance, analyze trends to anticipate issues, and drive improvements that enhance reliability, yield, and product quality. The role collaborates closely with Maintenance, Quality, Validation, and Manufacturing to coordinate spare‑parts strategies, preventative maintenance, calibration schedules, and implementation of clean‑in‑place systems. In a CDMO setting, the engineer also partners with clients and internal teams to support tech transfers, scale‑up activities, and lifecycle management of spray‑drying processes.\n","hostedUrl":"https://jobs.lever.co/seranbio/afe675bc-c9b1-4d19-911d-1a2280e61ed7","applyUrl":"https://jobs.lever.co/seranbio/afe675bc-c9b1-4d19-911d-1a2280e61ed7/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    \n
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    \n
    ","categories":{"commitment":"Full-time Exempt","department":"Process and Product Development","location":"Bend, Oregon","team":"Process and Product Development","allLocations":["Bend, Oregon"]},"createdAt":1775504575962,"descriptionPlain":"Serán seeks a Senior Scientist to join the Analytical Sciences group to play a key role in analytical characterization and method development for novel pharmaceutical drug products. This role supports process and process development by serving as a technical leader within the laboratory, driving method development, troubleshooting analytical challenges, interpreting complex data sets, and integrating analytical strategies across programs. The Senior Scientist independently designs experimental plans, authors reports, leads cross-functional discussions, and ensures scientific rigor across analytical deliverables. This position routinely interacts with internal and external partners, represents the analytical function in project teams, and contributes strategically to development programs.\n","description":"

    Serán seeks a Senior Scientist to join the Analytical Sciences group to play a key role in analytical characterization and method development for novel pharmaceutical drug products. This role supports process and process development by serving as a technical leader within the laboratory, driving method development, troubleshooting analytical challenges, interpreting complex data sets, and integrating analytical strategies across programs. The Senior Scientist independently designs experimental plans, authors reports, leads cross-functional discussions, and ensures scientific rigor across analytical deliverables. This position routinely interacts with internal and external partners, represents the analytical function in project teams, and contributes strategically to development programs.

    ","id":"ee61a753-3a1d-4f24-a5a6-7c4cb0adb849","lists":[{"text":"Duties and Responsibilities","content":"\n
  • Independently performs and interprets data for analytical techniques including HPLC, sink dissolution, Karl Fischer, XRD, and DSC
    • \n
  • Independently develops analytical protocols, data templates, and experimental plans that align with program needs and analytical test methods
    • \n
  • Develops and manages experimental workplans, timelines, and priorities for assigned projects
    • \n
  • Interprets analytical data, identifies trends, proposes hypotheses, and recommends next steps
    • \n
  • Authors technical reports and presentations with minimal guidance and contributes to regulatory-supporting documentation as needed
    • \n
  • Leads troubleshooting efforts on instruments and analytical workflows; contributes to laboratory instrumentation strategy, maintenance planning, and continuous lab improvements
    • \n
  • Serves as the analytical lead for cross-functional project teams, independently representing the analytical function to internal stakeholders and external partners
    • \n
  • Ensures all work complies with laboratory best practices, safety standards, and development SOPs
    • \n
  • May have direct reports with assumed supervisory responsibilities
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n\n
     
    "},{"text":"Required Skills and Abilities ","content":"
    \n\n
  • Extensive experience with HPLC and strong hands-on laboratory skills
    • \n
  • Preferred experience with Waters Empower
    • \n
  • Strong data interpretation skills
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Excellent verbal and written communication skills with the ability to communicate across technical levels
    • \n
  • Strong organizational and time management skills with a proven ability to manage multiple priorities and meet deadlines
    • \n
  • Demonstrated ability to work cross‑functionally in fast‑paced environments
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n\n
    "},{"text":"Education and Experience ","content":"
    \n\n
  • B.S. in Chemistry, Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related discipline with 5+ years of relevant experience;
    or
    • \n
  • M.S. in Chemistry, Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related discipline with 3+ years of relevant experience;
    or
    • \n
  • Ph.D. in Chemistry, Analytical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related discipline
    • \n
  • GMP experience not required
    • \n\n
    "},{"text":"Physical Requirements ","content":"
    \n\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 25 pounds occasionally
    • \n
  • Motor skills required for basic laboratory operations (pouring liquids, using utensils to transfer powders, visual assessments)
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n\n
    "}],"text":"Senior Scientist","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"

    Serán seeks a Senior Scientist to join the Analytical Sciences group to play a key role in analytical characterization and method development for novel pharmaceutical drug products. This role supports process and process development by serving as a technical leader within the laboratory, driving method development, troubleshooting analytical challenges, interpreting complex data sets, and integrating analytical strategies across programs. The Senior Scientist independently designs experimental plans, authors reports, leads cross-functional discussions, and ensures scientific rigor across analytical deliverables. This position routinely interacts with internal and external partners, represents the analytical function in project teams, and contributes strategically to development programs.

    ","descriptionBodyPlain":"Serán seeks a Senior Scientist to join the Analytical Sciences group to play a key role in analytical characterization and method development for novel pharmaceutical drug products. This role supports process and process development by serving as a technical leader within the laboratory, driving method development, troubleshooting analytical challenges, interpreting complex data sets, and integrating analytical strategies across programs. The Senior Scientist independently designs experimental plans, authors reports, leads cross-functional discussions, and ensures scientific rigor across analytical deliverables. This position routinely interacts with internal and external partners, represents the analytical function in project teams, and contributes strategically to development programs.\n","hostedUrl":"https://jobs.lever.co/seranbio/ee61a753-3a1d-4f24-a5a6-7c4cb0adb849","applyUrl":"https://jobs.lever.co/seranbio/ee61a753-3a1d-4f24-a5a6-7c4cb0adb849/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n \nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n \nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n \nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Process and Product Development","location":"Bend, Oregon","team":"Process and Product Development","allLocations":["Bend, Oregon"]},"createdAt":1769547516920,"descriptionPlain":"Serán seeks to hire a Senior Scientist to join the Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. This role will design products that meet the target product profiles defined by the project sponsor. To accomplish this, they will select the type of formulation approach and propose different prototype variations for manufacturing and testing. They will design experiments to guide the overall formulation approach and to evaluate different prototypes. Additionally, they will collaborate with analytical science and process development experts to form a comprehensive product team.\n \n","description":"
    Serán seeks to hire a Senior Scientist to join the Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. This role will design products that meet the target product profiles defined by the project sponsor. To accomplish this, they will select the type of formulation approach and propose different prototype variations for manufacturing and testing. They will design experiments to guide the overall formulation approach and to evaluate different prototypes. Additionally, they will collaborate with analytical science and process development experts to form a comprehensive product team.
    \n
     
    ","id":"22f257cc-ac4b-4e33-ad4d-50b426ef9dfd","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Independently develops experimental protocols and templates based on project need
    • \n
  • Independently summarizes, reports, and analyzes data to draw conclusions and proposes next steps
    • \n
  • Identifies out of trend data, forms hypothesis and investigates
    • \n
  • Evaluates data and draws conclusions across data sets/projects
    • \n
  • Contributes to laboratory, instrument, and/or equipment maintenance and coordination
    • \n
  • Communicates technical information to internal team
    • \n
  • Independently communicates technical information to external partners
    • \n
  • Authors technical reports and presentations with minimal guidance
    • \n
  • Develops and manages workplans
    • \n
  • May supervise and mentor teams
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n
  • Performs other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Scientific curiosity and willingness to learn
    • \n
  • Demonstrated experience in formulation sciences and drug product development
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrated ability to collaborate and work in cross-functional teams
    • \n
  • Demonstrated experience with advanced laboratory and data analysis skills
    • \n
  • Strong analytical and problem-solving skills
    • \n
  • Ability to prioritize tasks and to delegate them when appropriate
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict 
    • \n"},{"text":"Education and Experience ","content":"\n
  • B.S. in Science or Engineering discipline with 5+ years of experience,
    • \n
  • M.S. in Science or Engineering discipline with 3+ years of experience, or
    • \n
  • PhD in Science or Engineering discipline
    • \n"},{"text":"Physical Requirements ","content":"\n
  • Prolonged periods of sitting or standing at a desk and working on a computer
    • \n
  • Must be able to lift up to 25 pounds regularly and up to 50 pounds occasionally
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n
  • Motor skills required for basic laboratory operations (pouring liquids, using utensils to transfer powders, visual assessments)
    • \n"}],"text":"Senior Scientist, Product Development","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán seeks to hire a Senior Scientist to join the Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. This role will design products that meet the target product profiles defined by the project sponsor. To accomplish this, they will select the type of formulation approach and propose different prototype variations for manufacturing and testing. They will design experiments to guide the overall formulation approach and to evaluate different prototypes. Additionally, they will collaborate with analytical science and process development experts to form a comprehensive product team.
    \n
     
    ","descriptionBodyPlain":"Serán seeks to hire a Senior Scientist to join the Product Development group and contribute as part of an interdisciplinary team to develop and scale-up pharmaceutical manufacturing processes. This role will design products that meet the target product profiles defined by the project sponsor. To accomplish this, they will select the type of formulation approach and propose different prototype variations for manufacturing and testing. They will design experiments to guide the overall formulation approach and to evaluate different prototypes. Additionally, they will collaborate with analytical science and process development experts to form a comprehensive product team.\n \n","hostedUrl":"https://jobs.lever.co/seranbio/22f257cc-ac4b-4e33-ad4d-50b426ef9dfd","applyUrl":"https://jobs.lever.co/seranbio/22f257cc-ac4b-4e33-ad4d-50b426ef9dfd/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nLevel and compensation will be based on experience.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

    Level and compensation will be based on experience.

    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

    Benefits Summary:
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.

    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Exempt","department":"Product Commercialization","location":"Bend, Oregon","team":"Commercial Manufacturing","allLocations":["Bend, Oregon"]},"createdAt":1769262228515,"descriptionPlain":"Serán BioScience is motivated to find an industry-experienced Validation Engineer to support the development of a new commercial manufacturing facility. The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer of manufacturing process from clinical to commercial site, and subsequent validation for process, cleaning, and computerized systems to support commercial distribution of non-sterile pharmaceutical products. Experience will determine title and salary, with preference given to applicants with over 8 years of experience with Oral Solid Dosage and an interest in leading teams. Those with less experience are encouraged to apply. \n \nAs a critical member of the Commercial Steering Committee, the Senior Validation Engineer will be responsible for planning and execution of CQ and validation projects. In order to perform this task, applicants require a thorough understanding of the manufacturing processes and systems as well as an understanding of all applicable regulations, guidelines, policies, procedures, and requirements. Successful candidates will understand that the development and execution of CQ and validation projects requires communication with internal and external cross functional teams. Demonstrated ability with effective communication is essential for identifying required information, alignment of strategies, and mitigation risks while maintaining good working relationships.\n","description":"
    Serán BioScience is motivated to find an industry-experienced Validation Engineer to support the development of a new commercial manufacturing facility. The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer of manufacturing process from clinical to commercial site, and subsequent validation for process, cleaning, and computerized systems to support commercial distribution of non-sterile pharmaceutical products. Experience will determine title and salary, with preference given to applicants with over 8 years of experience with Oral Solid Dosage and an interest in leading teams. Those with less experience are encouraged to apply.
     
    As a critical member of the Commercial Steering Committee, the Senior Validation Engineer will be responsible for planning and execution of CQ and validation projects. In order to perform this task, applicants require a thorough understanding of the manufacturing processes and systems as well as an understanding of all applicable regulations, guidelines, policies, procedures, and requirements. Successful candidates will understand that the development and execution of CQ and validation projects requires communication with internal and external cross functional teams. Demonstrated ability with effective communication is essential for identifying required information, alignment of strategies, and mitigation risks while maintaining good working relationships.
    ","id":"a2cab472-b096-4ac4-bf53-3a582b1217f3","lists":[{"text":"Duties and Responsibilities ","content":"
  • Leads the commissioning and qualification (C&Q) of new and existing equipment and systems for OSD manufacturing, facilities, and utilities, ensuring compliance with cGMP, FDA, and EU regulatory standards
  • Supports the clinical technology transfer and operations in design, scale-up, optimization, and troubleshooting of OSD processes and equipment
  • Develops and executes protocols for equipment IQ/OQ/PQ in alignment with site validation master plans and project timelines
  • Collaborates with cross-functional teams to define equipment specifications, user requirements (URS), and establish project timelines and budgets
  • Manages installation activities, equipment FAT/SAT execution, and vendor coordination to ensure technical and compliance requirements are met
  • Collaborates with multidisciplinary team to complete change controls, deviations investigations, and CAPAs as required
  • Supports regulatory inspections and client audits
  • Performs other related duties as assigned
  • Responsibilities may increase in scope to align with company initiatives
    • "},{"text":"Required Skills and Abilities","content":"
  • Demonstrates knowledge of cGMPs guidelines and regulations acquired through education, experience, and training
  • Preference for those who posses knowledge of Global Regulatory requirements (E.g., FDA / MHRA / EMEA)
  • Showcases foundational understanding of the compliance and technical requirements for the application of various scientific concepts used in developing different dosage forms of pharmaceutical products (primarily oral solid dose, while experience with sterile products is desired)
  • Experience with regulatory expectations and industry practices for CQ and Validation using Product Lifecycle approach
  • Experience with designing CQV plans for Facilities, Utilities, and Process equipment desired
  • Ability to manage multiple projects, create and work within internal timeliness, solve problems, deliver on commitments, and utilize interpersonal skills in a cross-functional team
  • Strong time-management skills and the ability to organize and coordinate multiple projects at once
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
  • Ability to prioritize tasks and to keep leadership apprised of performance timelines
  • Accepts feedback from a variety of sources and constructively manages conflict
  • Demonstrates leadership skills with ability to motivate and coach cross functional teams
  • Experience in FAT/SAT of process equipment, and knowledge operating principles of typical OSD process equipment preferred.
  • Proficiency in enterprise systems, Microsoft Office, and other office productivity tools, with aptitude to learn new software and systems
    • "},{"text":"Education and Experience ","content":"
  • Bachelor's degree in relevant technical field
  • Requires a minimum of 8 years of quality, validation, or engineering experience in non-sterile clinical and commercial pharmaceutical manufacturing
  • Fundamental understanding of process equipment, utilities, manufacturing process, cleaning process and Quality systems used in the pharmaceutical/biotech industry
  • 8 years of GMP compliance experience, including knowledge of 21 CFR Part 11 requirements, GAMP 5, among others
    • "},{"text":"Physical Requirements ","content":"
  • Prolonged periods of sitting or standing at a desk and working on a computer
  • Prolonged periods of sitting or standing in a manufacturing environment
  • Must be able to lift fifteen pounds at times
  • Adheres to consistent and predictable in-person attendance
    • "}],"text":"Senior Validation Engineer","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is motivated to find an industry-experienced Validation Engineer to support the development of a new commercial manufacturing facility. The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer of manufacturing process from clinical to commercial site, and subsequent validation for process, cleaning, and computerized systems to support commercial distribution of non-sterile pharmaceutical products. Experience will determine title and salary, with preference given to applicants with over 8 years of experience with Oral Solid Dosage and an interest in leading teams. Those with less experience are encouraged to apply.
     
    As a critical member of the Commercial Steering Committee, the Senior Validation Engineer will be responsible for planning and execution of CQ and validation projects. In order to perform this task, applicants require a thorough understanding of the manufacturing processes and systems as well as an understanding of all applicable regulations, guidelines, policies, procedures, and requirements. Successful candidates will understand that the development and execution of CQ and validation projects requires communication with internal and external cross functional teams. Demonstrated ability with effective communication is essential for identifying required information, alignment of strategies, and mitigation risks while maintaining good working relationships.
    ","descriptionBodyPlain":"Serán BioScience is motivated to find an industry-experienced Validation Engineer to support the development of a new commercial manufacturing facility. The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer of manufacturing process from clinical to commercial site, and subsequent validation for process, cleaning, and computerized systems to support commercial distribution of non-sterile pharmaceutical products. Experience will determine title and salary, with preference given to applicants with over 8 years of experience with Oral Solid Dosage and an interest in leading teams. Those with less experience are encouraged to apply. \n \nAs a critical member of the Commercial Steering Committee, the Senior Validation Engineer will be responsible for planning and execution of CQ and validation projects. In order to perform this task, applicants require a thorough understanding of the manufacturing processes and systems as well as an understanding of all applicable regulations, guidelines, policies, procedures, and requirements. Successful candidates will understand that the development and execution of CQ and validation projects requires communication with internal and external cross functional teams. Demonstrated ability with effective communication is essential for identifying required information, alignment of strategies, and mitigation risks while maintaining good working relationships.\n","hostedUrl":"https://jobs.lever.co/seranbio/a2cab472-b096-4ac4-bf53-3a582b1217f3","applyUrl":"https://jobs.lever.co/seranbio/a2cab472-b096-4ac4-bf53-3a582b1217f3/apply"},{"additionalPlain":"Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.\n\nApplicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.\n\nBenefits Summary:\nSerán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.\n\nThe Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701\n","additional":"
    Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
    \n
     
    \n
    Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
    \n
     
    \n
    Benefits Summary:
    \n
    Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.
    \n
     
    \n
    The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
    ","categories":{"commitment":"Full-time Non-exempt","department":"Administrative and Business Development","location":"Bend, Oregon","team":"Finance","allLocations":["Bend, Oregon"]},"createdAt":1780095165925,"descriptionPlain":"Serán BioScience is searching for an experienced Staff Accountant to join the finance team. In this role you will prepare and maintain financial records to track the organization's assets, liabilities, profit and loss, tax liabilities and other related financial activities. Supported by the larger accounting department, the ideal candidate will have at least three years of related accounting experience to apply towards this position. Examples include maintaining a general ledger and preparing monthly P&L statements for internal stakeholders to review. Title and salary will be adjusted to meet the skills and abilities of selected candidate. Those with a degree in Accounting or similar field encouraged to apply. \n","description":"
    Serán BioScience is searching for an experienced Staff Accountant to join the Accounting and Finance team. In this role you will prepare and maintain financial records to track the organization's assets, liabilities, profit and loss, tax liabilities and other related financial activities. Supported by the larger Accounting Department, the ideal candidate will have at least three years of related accounting experience to apply towards this position. Examples include maintaining a general ledger and preparing monthly P&L statements for internal stakeholders to review. Title and salary will be adjusted to meet the skills and abilities of selected candidate. Those with a degree in Accounting or similar field encouraged to apply.
    ","id":"7f0ab68d-a7b0-4614-a829-f28c7bf1dcd1","lists":[{"text":"Duties and Responsibilities ","content":"\n
  • Performs general accounting and other related duties for the organization, including journal entries, account reconciliations, and month end closing task management
    • \n
  • Prepares monthly balance sheets and income (P&L) statements
    • \n
  • Maintains the general ledger
    • \n
  • May occasionally code invoices and sets up new accounts
    • \n
  • Reconciles accounts and helps close the monthly books
    • \n
  • Reconciles bank accounts monthly, verifies deposits, and addresses inquiries from banks
    • \n
  • Reconciles company credit cards monthly, monitors spending daily
    • \n
  • Reconciles cash disbursement accounts, payroll, customer accounts, and other financial accounts
    • \n
  • Provides outside auditors with assistance; gathers necessary account information and documents to perform annual audit
    • \n
  • Responsible for the creation of sales orders within SAP and daily communication with program management team on project status
    • \n
  • Files tax forms with federal, state, and local government agencies
    • \n
  • Co-manages the purchasing and invoicing system
    • \n
  • Maintains knowledge of acceptable accounting practices and procedures
    • \n
  • Responsibilities may increase in scope to align with company initiatives
    • \n
  • Performs other related duties as assigned
    • \n"},{"text":"Required Skills and Abilities ","content":"\n
  • Excellent verbal and written communication skills
    • \n
  • Excellent organizational skills and attention to detail
    • \n
  • Knowledge of general financial accounting and cost accounting
    • \n
  • Understanding of and the ability to adhere to generally accepted accounting principles
    • \n
  • Ability to correctly prepare month end financial statements
    • \n
  • Excellent time management skills with a proven ability to meet deadlines
    • \n
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
    • \n
  • Demonstrates the ability to collaborate and work in cross-functional teams
    • \n
  • Accepts feedback from a variety of sources and constructively manages conflict
    • \n
  • Ability to function well in a high-paced and at times stressful environment
    • \n
  • Proficient with Microsoft Office Suite or similar software, and ERP management experience
    • \n"},{"text":"Education and Experience ","content":"\n
  • Bachelor’s degree in Accounting, or related field, required
    • \n
  • At least three years of related experience required
    • \n
  • Working knowledge of SAP preferred
    • \n"},{"text":"Physical Requirements","content":"\n
  • Prolonged periods sitting at a desk and working on a computer
    • \n
  • Must be able to lift up to 15 pounds at times
    • \n
  • Adheres to consistent and predictable in-person attendance
    • \n"}],"text":"Staff Accountant","country":"US","workplaceType":"onsite","opening":"","openingPlain":"","descriptionBody":"
    Serán BioScience is searching for an experienced Staff Accountant to join the Accounting and Finance team. In this role you will prepare and maintain financial records to track the organization's assets, liabilities, profit and loss, tax liabilities and other related financial activities. Supported by the larger Accounting Department, the ideal candidate will have at least three years of related accounting experience to apply towards this position. Examples include maintaining a general ledger and preparing monthly P&L statements for internal stakeholders to review. Title and salary will be adjusted to meet the skills and abilities of selected candidate. Those with a degree in Accounting or similar field encouraged to apply.
    ","descriptionBodyPlain":"Serán BioScience is searching for an experienced Staff Accountant to join the finance team. In this role you will prepare and maintain financial records to track the organization's assets, liabilities, profit and loss, tax liabilities and other related financial activities. Supported by the larger accounting department, the ideal candidate will have at least three years of related accounting experience to apply towards this position. Examples include maintaining a general ledger and preparing monthly P&L statements for internal stakeholders to review. Title and salary will be adjusted to meet the skills and abilities of selected candidate. Those with a degree in Accounting or similar field encouraged to apply. \n","hostedUrl":"https://jobs.lever.co/seranbio/7f0ab68d-a7b0-4614-a829-f28c7bf1dcd1","applyUrl":"https://jobs.lever.co/seranbio/7f0ab68d-a7b0-4614-a829-f28c7bf1dcd1/apply"}]