• Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …or continued marketing. **Job Description** + Develop and implement global CMC regulatory strategies for late-stage development, marketing applications (eg, ... of regulatory submissions (IND/IMPD/NDA/MAA, post-approval supplements). Determine regulatory CMC content and scientific/technical requirements to ensure… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Specialist, Digital CMC

    Merck (Boston, MA)
    …development through commercialization, with practical insight into how these operations generate CMC regulatory content + Understanding of CMC operations, ... source systems to regulatory documentation. Under the guidance of dCMC Regulatory Authoring Leadership, the Senior Specialist, Regulatory Authoring… more
    Merck (12/02/25)
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  • Senior Manager of Statistics-…

    Takeda Pharmaceuticals (Cambridge, MA)
    …innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Manager of Statistics- CMC in our Cambridge, MA office. As a ... Senior Manager of Statistics, you will provide statistical leadership in...design, analysis, and interpretation of Chemicals, Manufacturing, and Controls ( CMC ) study data throughout Pharmaceutical Sciences. We seek an… more
    Takeda Pharmaceuticals (12/03/25)
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  • Senior Manager , Global…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …business units as needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Manager , Global Product…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    The Senior Manager , Global Product Quality - Biologics is responsible for managing quality oversight of clinical and commercial products at CMOs under contract ... submissions for OPDC R&D products. Performs quality reviews of CMC sections of regulatory submissions. + Authors...of combined experience in pharmaceutical/medical device industry as a manager in Manufacturing, QA or QC role supporting GMP… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Senior Director, Global Program Leader…

    Takeda Pharmaceuticals (Boston, MA)
    …company that will inspire you and empower you to shine? Join us as a Senior Director, Global Program Leader - Oncology, Solid Tumors in our Cambridge office. At ... experienced, versatile and strong enterprise leaders + Committed to simultaneously driving regulatory approval as well as launch and global patient access + Ability… more
    Takeda Pharmaceuticals (10/23/25)
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  • Sr. Non-Clinical Biostatistician

    Sanofi Group (Waltham, MA)
    …Functional Planner, Project Manager , CROs, etc.) + Under supervision of the senior manager of the TED team or Research lead, participates in project ... diseases and bring hope to patients and their families. The Biostatistics Manager of the TED (Translational and Early Development) team supports Vaccine R&D… more
    Sanofi Group (11/25/25)
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