• Associate Director

    Lilly (Boston, MA)
    …treatment from chronic management to single-course gene editing medicines. **Position Summary:** The Associate Director , Regulatory CMC will work closely ... subject matter experts to provide strategic and operational input for CMC regulatory activities including submissions, reviews, and health authority… more
    Lilly (01/16/26)
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  • Associate Director

    Sumitomo Pharma (Boston, MA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She...the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of… more
    Sumitomo Pharma (01/10/26)
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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** ... 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 , Principal…

    Bristol Myers Squibb (Devens, MA)
    …more: careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), in ... of your application should be directed to Chat with Ripley. R1597688 : Associate Director , Principal Product Quality Lead **Company:** Bristol-Myers Squibb **Req… more
    Bristol Myers Squibb (01/10/26)
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  • Process Engineer Small Molecules API Process…

    Takeda Pharmaceuticals (Boston, MA)
    …**Job Description** **Title: Process Engineer Small Molecules API Process Science ( Associate Director )** **Location: Cambridge, MA (Hybrid)** **About the role:** ... As a Process Engineer Small Molecules API Process Science ( Associate Director ), you will provide process engineering...+ Other key functional groups such as Global Quality, Regulatory CMC etc. **Leadership** + Provide vision… more
    Takeda Pharmaceuticals (12/16/25)
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  • Associate Director , API Process…

    Takeda Pharmaceuticals (Cambridge, MA)
    …true 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 ... strategy), site leadership, Technical Services, Pharmaceutical Sciences, Global Quality, and Regulatory CMC . + Provide technical support to marketing… more
    Takeda Pharmaceuticals (11/25/25)
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  • Associate Director , Genomic…

    Sanofi Group (Waltham, MA)
    **Job Title:** Associate Director , Genomic Medicine Purification Process Development **Location:** Waltham, MA Work Model: M-F onsite **About the Job** Are you ... our teams accelerate progress. The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment...Group located in Waltham, MA in the role of Associate Director . The GMU PPD group operates… more
    Sanofi Group (11/05/25)
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  • Process Scientist ( Associate

    Takeda Pharmaceuticals (Boston, MA)
    …DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), ... and the life cycle management of existing products. You will lead regulatory interactions, including the preparation of Chemistry, Manufacturing, and Controls (… more
    Takeda Pharmaceuticals (12/19/25)
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