• Takeda Pharmaceuticals (Lexington, MA)
    site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC . Provide technical support to marketing applications for ... to the 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 API… more
    job goal (12/12/25)
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  • 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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  • Senior Director , Global Regulatory

    Bristol Myers Squibb (Cambridge, MA)
    …at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Sr Director , Global Regulatory Strategy, Neuroscience** + Will be a key ... Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area. + Acts… more
    Bristol Myers Squibb (11/13/25)
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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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  • Associate Director , API Process…

    Takeda Pharmaceuticals (Cambridge, 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 (09/16/25)
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  • Executive Director , Global Program Lead…

    Bristol Myers Squibb (Cambridge, MA)
    …late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision ... for both internal and external opportunities. + Participates in regulatory filings (NDA, BLA filings) as well as develops...evidence. + Supports commercial needs and recommendations to guide CMC and GPS on trade packaging and commercial product.… more
    Bristol Myers Squibb (11/20/25)
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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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