• Regulatory Affairs Program

    Olympus Corporation of the Americas (Westborough, MA)
    …of a high-growth, innovative team, this position oversees collaboration between internal Olympus Regulatory Affairs Teams and external vendors as needed and will ... comparable required. + Minimum of 10 years' experience in Regulatory Affairs , ideally within the medical device...coverage effective on start date + 24/7 Employee Assistance Program + Free live and on-demand Wellbeing Programs +… more
    Olympus Corporation of the Americas (11/07/25)
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  • Senior Manager , Regulatory

    Olympus Corporation of the Americas (Westborough, MA)
    …supports the Global Senior Manager to plan and direct the OSTA Core Regulatory Affairs Team activities including but not limited to analysis of requirements ... medical devices. This leadership role leads an OSTA Core Regulatory Affairs Team and provides world-class ...coverage effective on start date + 24/7 Employee Assistance Program + Free live and on-demand Wellbeing Programs +… more
    Olympus Corporation of the Americas (11/07/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Cambridge, MA)
    …more: careers.bms.com/working-with-us . **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for ... Solid scientific background, PhD., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years. + Scientific… more
    Bristol Myers Squibb (11/24/25)
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  • Global Lead - Medical Affairs

    Olympus Corporation of the Americas (Westborough, MA)
    …(https://www.olympusamerica.com/careers) . **Job Description** The Global Lead Medical Affairs - Gastroenterology (GLMAG) is a board-certified, fellowship trained ... proficient in endoscopy with deep clinical practice knowledge, medical affairs industry experience, and/or health leadership competencies and management… more
    Olympus Corporation of the Americas (11/21/25)
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  • Regulatory CMC Project Manager

    Parexel (Boston, MA)
    If you are passionate about regulatory affairs and project management, and are looking for a challenging and rewarding opportunity, we would love to hear from ... dedicated client partnership and play a pivotal role in their regulatory affairs department. Key Responsibilities: Collaborative Coordination: Work closely… more
    Parexel (01/09/26)
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  • Regulatory Operations Manager

    Dana-Farber Cancer Institute (Boston, MA)
    …in collaboration with key stakeholders + Meet regularly with program manager (s) to review and collaborate regarding regulatory workload prioritization. Work ... the CTIP Associate Director for the Pediatric unit, the Regulatory Operations Manager (ROM) will oversee the...start-up, active and close-out phases + Proficient knowledge of regulatory affairs , research ethics and the responsible… more
    Dana-Farber Cancer Institute (01/02/26)
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  • Senior Manager , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …order to bring life-changing therapies to patients worldwide. Join Takeda as Senior Manager , Global Regulatory Labeling Strategy where you will be responsible ... negotiations with Health Authorities. + Ensures labeling content conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (01/15/26)
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  • Summer Regulatory Projects & Compliance…

    Eversource Energy (Westwood, MA)
    …requires interaction with a myriad of individuals within the Companies \(e\.g\., legal, regulatory affairs , business owners\) + Regulatory Analysts work ... position is responsible for working across Eversource to identify and respond to regulatory obligations in as established by law and the Regulatory Authorities… more
    Eversource Energy (01/15/26)
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  • Lead SaMD Technical Program Manager

    Wolters Kluwer (Waltham, MA)
    The **Principal SaMD Technical Program Manager ** plays a pivotal role in driving the development and delivery of Software as a Medical Device (SaMD) products. ... The Principal SaMD TPM acts as a bridge between engineering, product, regulatory affairs , clinical, and quality assurance teams, facilitating strategic… more
    Wolters Kluwer (12/04/25)
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  • Senior Program Manager , Strategic…

    Eversource Energy (Westwood, MA)
    …J\-1, O\-1, etc\.\)\. **Our Team** Eversource is looking for a **Senior Program Manager , Strategic Project Development, Transmission** located in **Westwood, ... and budgets in the conceptual phase prior to execution + Interacts regularly with Regulatory Affairs , Environmental Affairs , and Energy Efficiency to develop… more
    Eversource Energy (12/30/25)
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