• 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 (08/28/25)
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  • Associate Director -Process Engineer SM API…

    Takeda Pharmaceuticals (Boston, MA)
    …Sciences counterparts. + o Other key functional groups such as Global Quality, Regulatory CMC etc. **Leadership** + Provide vision and strategy for manufacturing ... true to the best of my knowledge. **Job Description** **Title: Associate Director -Process Engineer SM API Process Sci** **Location: Cambridge, MA (Hybrid)** **About… more
    Takeda Pharmaceuticals (09/16/25)
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  • Executive Director , Global Development…

    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 (10/18/25)
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  • GRA Device Lead (Associate Director )

    Sanofi Group (Cambridge, MA)
    …(60% on- site ) and comprehensive well-being programs. + Influence global regulatory strategies, interact with key health authorities, and stay at the forefront ... **Job Title:** GRA Device Lead (Associate Director ) **Location** : Morristown, NJ/ Cambridge, MA/ Framingham,...critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse… more
    Sanofi Group (09/23/25)
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  • GRA Device Lead (Associate Director )

    Sanofi Group (Cambridge, MA)
    …(60% on- site ) and comprehensive well-being programs. + Influence global regulatory strategies, interact with key health authorities, and stay at the forefront ... **Job Title:** GRA Device Lead (Associate Director ) **Location:** Cambridge, MA/ Morristown, NJ **About the...critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse… more
    Sanofi Group (09/20/25)
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