• GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/20/25)
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  • Nursing Assistant

    Veterans Affairs, Veterans Health Administration (Bedford, MA)
    …Massachusetts. This announcement is intended to fill multiple vacancies throughout the Veterans Affairs Medical Center in Bedford, MA. Available shifts could be ... is located in the Nursing Service (Mental Health) at the Bedford VA Healthcare Medical Center, in Bedford, Massachusetts. This is a full time position at 40-hours… more
    Veterans Affairs, Veterans Health Administration (11/07/25)
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  • Project Manager, Med Device , R&D PMO,…

    Eliassen Group (Boston, MA)
    …http://careers.eliassen.com/iXUiCO + Description + Recommended Jobs **Description:** Our Fortune 500 Medical Device client is seeking a Project Manager to ... risk management, and communication across all stakeholders. * Coordinate with Regulatory Affairs to ensure documentation and submission readiness for… more
    Eliassen Group (10/25/25)
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  • Vice President, Internal Medicine…

    Pfizer (Cambridge, MA)
    …industry, preferably in Drug Development or Clinical Research, ideally within Regulatory Affairs + Subject-matter expertise within assigned therapeutic area ... to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Regulatory Affairs more
    Pfizer (11/13/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Quality Engineer II - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …communicating testing activities. The role works with Product Development, Project Management, Regulatory , Marketing and Medical Affairs . **ESSENTIAL DUTIES ... in close collaboration with Product Development, Project Management, RA, Marketing and Medical Affairs . Support Design Reviews, Technical Reviews, and Gate… more
    Integra LifeSciences (09/06/25)
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  • Director, Global Regulatory Labeling…

    Takeda Pharmaceuticals (Boston, MA)
    …represented at the Labeling cross functional teams, including clinical, safety, medical affairs , and commercial, to ensure unparalleled communication ... bring life-changing therapies to patients worldwide. Join Takeda as Director, Global Regulatory Labeling Strategy where you will be responsible for the development… more
    Takeda Pharmaceuticals (11/16/25)
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  • Principal Engineer, Design Quality - Software

    Olympus Corporation of the Americas (Westborough, MA)
    …subject matter expertise, technical guidance, and leadership for the application of health and medical device SW regulatory standards to the Olympus SDLC, ... projects as required by the SDLC and will support Regulatory Affairs ' efforts in creating submission materials...on regulations around health software development, and software for medical devices . + Collaborate on the update… more
    Olympus Corporation of the Americas (11/13/25)
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  • Senior Specialist, Medical Writing

    Edwards Lifesciences (Boston, MA)
    …Bachelor's Degree in a related field with 5 years of related experience working in medical affairs , clinical affairs and/or clinical science **What else we ... internal/external working relationships + The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment… more
    Edwards Lifesciences (09/27/25)
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  • Lead Design Assurance Engineer

    Hologic (Marlborough, MA)
    …Are you passionate about driving innovation while ensuring compliance and quality in medical device development? At Hologic, we are seeking a **Lead Design ... and a commitment to delivering safe, reliable, and durable medical devices , we want to hear from...+ Collaborative and team-oriented, building strong relationships across R&D, Regulatory Affairs , Manufacturing, and other key stakeholders.… more
    Hologic (10/30/25)
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