• Director , Regulatory Site

    Takeda Pharmaceuticals (Boston, MA)
    …of what is possible in order to bring life-changing therapies to patients worldwide. The Director Regulatory Site CMC ensures efficient and compliant ... based on risk and scientific rationale. + Facilitate alignment between site teams and global Regulatory CMC on post-approval strategies and activities and… more
    Takeda Pharmaceuticals (12/10/25)
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  • Global Regulatory Affairs Device Lead…

    Sanofi Group (Framingham, MA)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** Are ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse...of products. The team is part of the GRA CMC & GRA Device Department within Global R&D. The… more
    Sanofi Group (10/23/25)
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  • Director , Vector Technical Program Lead

    Bristol Myers Squibb (Devens, MA)
    …to ensure product quality, compliance and supply. + Author, review and approve regulatory CMC submission sections. + Drive continuous improvement initiatives to ... influencing external partnerships (CDMOs/CMOs) to achieve strategic outcomes. + Knowledge of CMC regulatory , drug substance & drug product manufacturing, and… more
    Bristol Myers Squibb (01/03/26)
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  • Associate Director , Principal Product…

    Bristol Myers Squibb (Devens, MA)
    CMC deliverables, technical team objectives, life-cycle improvements, and regulatory commitments. + Provides technical quality expertise and compliance oversight ... . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), in Global Product Quality… more
    Bristol Myers Squibb (01/01/26)
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  • Associate Director , API Process…

    Takeda Pharmaceuticals (Lexington, MA)
    site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC . + Provide technical support to marketing applications for ... best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global expert for small-molecule… more
    Takeda Pharmaceuticals (11/25/25)
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  • Process Engineer Small Molecules API Process…

    Takeda Pharmaceuticals (Boston, MA)
    …Pharmaceutical Sciences counterparts. + Other key functional groups such as Global Quality, Regulatory CMC etc. **Leadership** + Provide vision and strategy for ... Description** **Title: Process Engineer Small Molecules API Process Science (Associate Director )** **Location: Cambridge, MA (Hybrid)** **About the role:** As a… more
    Takeda Pharmaceuticals (12/16/25)
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  • Director / Senior Director , Nucleic…

    Alloy Therapeutics (Waltham, MA)
    …the global organization to always maintain our nimble, startup culture. This is an on- site and full-time position in Waltham, MA. At Alloy, we have an ethos of ... with external partners to discover and develop AntiClastic RNA medicines. The Role The Director to Executive Director of Nucleic Acid Chemistry will lead a team… more
    Alloy Therapeutics (12/04/25)
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