• 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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  • 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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  • 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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