• Associate Director, Search & Evaluation

    AbbVie (Cambridge, MA)
    …group is part of the Corporate Strategy Office and actively supports global Business Development (BD) goals by sourcing and assessing external partnering ... invest into- or acquire assets. The group is responsible for leading the global search efforts for assets of high strategic value across the entire spectrum,… more
    AbbVie (05/28/25)
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  • Chief Operating Officer (CRO/Pharma/Device)

    Actalent (Boston, MA)
    …have a strong background in business management, clinical research, and regulatory affairs , with a commitment to enhancing service delivery through innovation and ... is anticipated to close on Aug 29, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary… more
    Actalent (08/16/25)
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  • Sr. Coordinator, Regulatory Submission Operations

    Cardinal Health (Boston, MA)
    …contributes to Cardinal Health_** Regulatory Submissions Operations provides regulatory affairs and product development consulting services to enable pharmaceutical, ... More specifically, this role serves the function to support global , post-approval lifecycle regulatory requirements for Biologics and small-chemical entity… more
    Cardinal Health (08/13/25)
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  • Regional Account Medical Lead (Associate Director)

    Takeda Pharmaceuticals (Boston, MA)
    …Takeda policies. .Lead effectively Field Medical Matrix partners (MSLs) and internal Medical Affairs experts to meet the need of key accounts for specialized or deep ... and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for… more
    Takeda Pharmaceuticals (08/12/25)
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  • Senior Medical Director

    Astrix Technology (Boston, MA)
    …strategy, including RNA, genomic, proteomic, and imaging-based markers. + Contribute to global regulatory submissions (eg, INDs, CTAs) and provide medical input in ... with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + Represent the… more
    Astrix Technology (08/11/25)
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  • AVP & Counsel, Advanced Markets

    Manulife (MA)
    …+ Support government relations and advocacy efforts in coordination with public affairs . **Required Qualifications:** + JD from an accredited law school; active ... where well-being and inclusion are more than just words. + As part of our global team, we'll support you in shaping the future you want to see. \#LI-Remote \#LI-JH… more
    Manulife (08/09/25)
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  • Senior Engineer, Design Transfer Specialist

    Amgen (Cambridge, MA)
    …the seamless transfer of product designs from our development site to various global manufacturing sites. This role requires a deep understanding of medical device ... with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs , to ensure alignment and successful design transfer. + **Vendor… more
    Amgen (08/08/25)
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  • Sr. QA Specialist, Operations

    Catalent Pharma Solutions (Chelsea, MA)
    …final products. **EDUCATION AND** **EXPERIENCE** : Requires a Bachelor's degree in Drug Regulatory Affairs and 4 years of experience in job offered or 4 years of ... Full Time **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000… more
    Catalent Pharma Solutions (07/24/25)
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  • Director, Market Access and Channel Strategy- PDT

    Takeda Pharmaceuticals (Boston, MA)
    …preferred + Experience working across Medical, Legal, Finance, Analytics, Public Affairs , etc. + Financial acumen including resource allocation, budget management ... and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for… more
    Takeda Pharmaceuticals (07/18/25)
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  • Senior Director, MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …the process validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process Verification ... + Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies and optimize product lifecycle… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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