• Cytiva (Marlborough, MA)
    …for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in ongoing ... delivery.What you'll do:Support the Business and Customers in a global environment by providing quality documents and...in Biochemistry/Chemistry or related field3+ years of experience in GMP , quality , product management or a related… more
    JobGet (06/08/25)
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  • Global Quality Lead

    Sanofi Group (Framingham, MA)
    **Job Title:** Global Quality Lead , GMP , GDP Audit and Inspection - Pipeline Launch **Location:** Framingham, MA or Morristown, NJ **About the Job** We ... in Sanofi. + **Scope:** Manufacturing & Supply, Research & Development, Countries, Digital, Global Quality organizations in Sanofi. And third parties outside of… more
    Sanofi Group (05/03/25)
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  • GMP Analytical Testing Lead - Cell…

    Eurofins (Cambridge, MA)
    …expectations. + Ensure all activities are conducted in strict accordance with GMP guidelines and quality standards. Leadership Responsibilities: + Supervise and ... are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in… more
    Eurofins (06/06/25)
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  • Director, Quality Assurance GMP

    Nitto Denko Corp. (Milford, MA)
    About this opportunity : The Director, Quality Assurance GMP Operations is responsible for quality oversight of the manufacturing process and operations. ... internal and external stakeholders to drive compliance and continuous improvement of GMP operations. Key Responsibilities + Provide quality expertise, oversight… more
    Nitto Denko Corp. (05/15/25)
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  • Validation Lead , Quality Assurance

    Astellas Pharma (Westborough, MA)
    **Validation Lead , Quality Assurance** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are ... is headquartered in Massachusetts. Astellas is announcing a **Validation Lead , Quality Assurance** opportunity at their **Astellas...policies and procedures and industry best practices. The Validation Lead will ensure that all critical GMP more
    Astellas Pharma (03/25/25)
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  • Executive Director, Cell Therapy Global

    Bristol Myers Squibb (Devens, MA)
    …External Manufacturing, Regulatory Affairs and Brand teams. The individual provides end-to-end global quality oversight of all cell therapy development programs ... for cell therapy commercial, clinical and development products. + Acts as lead Quality management reviewer/approver of regulatory submissions and responses to… more
    Bristol Myers Squibb (05/25/25)
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  • Lead Quality Specialist

    ThermoFisher Scientific (Franklin, MA)
    …support business needs.** **A Day in the Life** **We are seeking a dedicated professional to lead GMP Quality Control (QC) and Quality Assurance (QA) ... to ensure procedures and specifications are well-developed and effectively implemented.** ** Lead process quality initiatives by monitoring trends, identifying… more
    ThermoFisher Scientific (05/31/25)
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  • Lead GMU Technical Operations

    Sanofi Group (Framingham, MA)
    …view. **Scope** + Sanofi R&D Sites/ platforms, interactions with CMC, R&D Vaccines, Global Quality , Alliance Management, Global Regulatory Affairs, Clinical ... families. The purpose of this position is to provide quality technical management oversight of Sanofi sponsored GMP... manufacturing and testing of genomic medicines. Specifically, to lead the following activities: + Manage the quality more
    Sanofi Group (05/29/25)
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  • Lead Quality Systems Auditor

    Fresenius Medical Center (Waltham, MA)
    … and Compliance, Collaboration, No-Limits Mindset and Results Oriented. **PURPOSE AND SCOPE:** Lead Quality Systems Auditor will act as a Subject Matter Expert ... plans, conducts, and leads audits in accordance with the global QS audit program + Lead and...in the interpretation of FDA guidelines, Good Manufacturing Practices ( GMP ) and relevant quality standards for pharmaceuticals… more
    Fresenius Medical Center (05/13/25)
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  • Director, Raw Material Strategy and Drug Product…

    Lilly (Boston, MA)
    …**Summary** We are looking for a proactive, scientifically grounded Director to lead the development and integration of GMP cell banking, cryopreserved ... to scale into future clinical phases. **Roles and Responsibilities** + Establish and lead a unified technical strategy that integrates GMP cell banking,… more
    Lilly (05/09/25)
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  • Associate Director, Technical Operations…

    Bristol Myers Squibb (Devens, MA)
    …as the Global Technical SME for Drug Product and Vector Validation. The lead will develop global technical standards for cell therapy validation and deploy ... providing SME assessment for proposed process life-cycle changes. The lead will serve as the Global Point...global cell therapy validation technical standards via the quality system. + Promote innovative and efficient approaches to… more
    Bristol Myers Squibb (06/04/25)
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  • Senior Director, Devens Digital Plant and Site IT…

    Bristol Myers Squibb (Devens, MA)
    …BioPharma Operating Units, the Sr. Director, BI&T, Devens Digital Plant and Site BI&T Lead will be directly accountable to the US Biologics Leader and Devens Campus ... a standing member of the Devens Campus leadership team. **Key Responsibilities:** + Lead a matrixed organization composed of both site direct reports and groups of… more
    Bristol Myers Squibb (04/20/25)
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  • Compliance Head, US FDA

    Sanofi Group (Framingham, MA)
    …and high- quality responses and support the development and promotion of Global Quality Documentation. + Supports the preparation, execution and closure of ... purposes, and ensuring accurate reporting to Operations Management and Global Quality . . **Core member of critical.... . **Core member of critical governance** + Sanofi's GMP GDP Quality Council to facilitate sharing… more
    Sanofi Group (06/03/25)
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  • Site Quality Head

    Curia (Hopkinton, MA)
    …and drives Quality decisions at the site and also supports regional Director of Quality for global Quality initiatives + Provides hands on leadership and ... and packaging operations + Responsible for all aspects of GMP compliance. This includes quality oversight from...continuous improvement efforts + Ensure applicable requirements of Curia global Quality Systems are implemented and maintained… more
    Curia (05/20/25)
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  • Head, Analytical Controls (Sr. Director)

    Takeda Pharmaceuticals (Lexington, MA)
    …etc. in conjunction with senior staff and global line and function heads + Lead global CMC and Quality key initiatives and represent Pharm Sci to ... my knowledge. **Job Description** **How you will contribute:** + Lead and develop a global team of...Stability and Shelf life; c) Reference Standard Management; d) GMP Quality Systems + Contribute to product… more
    Takeda Pharmaceuticals (06/06/25)
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  • Principal Quality Engineer

    Medtronic (Billerica, MA)
    …and compensation plans (https://www3.benefitsolver.com/benefits/BenefitSolverView?page\_name=signon&co\_num=30601&co\_affid=medtronic) We lead global healthcare ... for this opening will close on - 11 Jun 2025 Position Description: Principal Quality Engineer for Medtronic, Inc located in Billerica, MA. Develop, modify, apply and… more
    Medtronic (04/08/25)
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  • Lead Contracts Manager - Data Center…

    Meta (Boston, MA)
    **Summary:** Meta seeks highly engaged and experienced team players for lead roles to join our Design, Engineering & Construction (DEC) organization to direct ... join a high-powered team of industry leaders! **Required Skills:** Lead Contracts Manager - Data Center Design, Engineering &...team, peers, and outside business units to enhance the quality and efficiency of contracting processes. 12. Ensure all… more
    Meta (06/03/25)
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  • Head of Analytical Development and Quality

    Cambrex High Point (Waltham, MA)
    …Chemistry's state of the art complex-synthetics route development. Additionally, they will lead and advance the Quality Control function, collaborating with ... with the oversight of both analytical development activities and execution of Quality Control responsibilities. They will lead the analytical team, interface… more
    Cambrex High Point (06/08/25)
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  • Quality Assurance Specialist III

    Nitto Denko Corp. (Milford, MA)
    …that the QA project team is well trained in phase appropriate GMPs, global GMP API regulations, directives and have familiarity with Avecia's manufacturing ... : In this role you will be responsible for interfacing with and provide quality input to client's manufacturing programs that are in early stages of development or… more
    Nitto Denko Corp. (05/24/25)
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  • Quality and Regulatory Support Manager

    Danaher Corporation (Marlborough, MA)
    …for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in ongoing ... do: + Support the Business and Customers in a global environment by providing quality documents and...or related field + 3+ years of experience in GMP , quality , product management or a related… more
    Danaher Corporation (04/01/25)
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