• Regulatory CMC Project

    Parexel (Boston, MA)
    …innovative treatment options to patients. We are currently seeking a dedicated and detail-oriented ** Regulatory CMC Project Manager ** to join a growing, ... requirements. Project Management: Serve as the project manager for meetings, adhering to best...Project Management). + 3+ years proven experience in regulatory affairs, particularly in CMC (Chemistry, Manufacturing,… more
    Parexel (12/12/25)
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  • Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …of regulatory guidelines and perspective to the cross-functional team. Serve as CMC regulatory lead on global project teams (Pharmaceutical Development, ... domestic/international travel. **Job Description** + Develop and implement global CMC regulatory strategies for late-stage development, marketing applications… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • CMC Project Manager

    Takeda Pharmaceuticals (Boston, MA)
    …application is true to the best of my knowledge. **Job Description** **Title: CMC Project Manager ** **Location: Cambridge, MA (Hybrid)** **About the ... role:** As a CMC Project Manager , you will...& discontinuation, launch execution & global expansion/contraction, COGs management, regulatory activities, product / process. + knowledge, capability &… more
    Takeda Pharmaceuticals (10/10/25)
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  • Senior Specialist, Digital CMC

    Merck (Boston, MA)
    …Informatica Metadata Manager , Management Process, Process Flow Documentation, Project Management, Regulatory Documents, SAP Master Data Governance (MDG), ... development through commercialization, with practical insight into how these operations generate CMC regulatory content + Understanding of CMC operations,… more
    Merck (12/02/25)
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  • Senior Manager of Statistics- CMC

    Takeda Pharmaceuticals (Cambridge, MA)
    …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 ... in the design, analysis, and interpretation of Chemicals, Manufacturing, and Controls ( CMC ) study data throughout Pharmaceutical Sciences. We seek an innovative and… more
    Takeda Pharmaceuticals (12/03/25)
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  • Global Manufacturing Sciences CMC Lead

    Takeda Pharmaceuticals (Lexington, MA)
    …approaches to reduce COGs and strengthen supply reliability. + Collaborate closely with an assigned CMC Project Manager (who will provide you PM support). + ... Site Manufacturing Sciences, QA, QC, Engineering, Supply Chain, Validation and Regulatory CMC to ensure aligned, efficient CMC execution across functions… more
    Takeda Pharmaceuticals (12/04/25)
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  • Senior Manager , Global Regulatory

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external...needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Manager , Commercial Biologics…

    Takeda Pharmaceuticals (Lexington, MA)
    …or more products and provide strong technical expertise and leadership for regulatory interactions, including authoring CMC content for multi-site products. ... and timely decision-making. + Represent Biologics Product Sciences on cross-functional CMC and project teams and collaborate closely with Pharmaceutical… more
    Takeda Pharmaceuticals (12/11/25)
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  • Senior Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    regulatory submissions for OPDC R&D products. Performs quality reviews of CMC sections of regulatory submissions. + Authors and maintains Standard Operating ... The Senior Manager , Global Product Quality - Biologics is responsible...Subsidiaries ensure Compliance with local and global requirements and regulatory requirements. + Interfaces with project teams… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Senior Director, Global Program Leader - Oncology,…

    Takeda Pharmaceuticals (Boston, MA)
    …experienced, versatile and strong enterprise leaders + Committed to simultaneously driving regulatory approval as well as launch and global patient access + Ability ... The GPL ensures through the functional sub-teams leaders and their teams all project deliverables achieve defined project scope & objectives, budget and… more
    Takeda Pharmaceuticals (10/23/25)
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  • Head of Material Planning

    Sanofi Group (Framingham, MA)
    …requirements for post approval changes and of information typically found in the CMC sections of regulatory submissions + Knowledge and experience with ... coverage targets as defined by Policy or Critical Material Manager (GSP) in case of exceptions / deviations *...and purchasing systems in a CGMP manufacturing environment + Project management skills + Expertise in document management systems… more
    Sanofi Group (10/28/25)
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