• Product Stewardship & Regulatory Expert…

    Chemours (Boston, MA)
    …Engineering, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw ... outside lawyers, consultants, industry associations, and local agencies on specific medical regulatory topics. + Coordinate and review customer… more
    Chemours (06/19/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Boston, MA)
    …+ Bachelors in related field, preferred + 2+ years' experience in Medical Device Regulatory Affairs/Quality experience preferred + Certification ... Private Brand, Presource, and Sustainable Technologies businesses and range of medical devices . + Maintain regulatory data, intelligence, and analytics… more
    Cardinal Health (07/09/25)
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  • Director or Regulatory , Software…

    Philips (Cambridge, MA)
    …the right fit if:** + You've acquired 10+ years of experience working in Regulatory Affairs within the medical device industry; Experience with ... **Director, Regulatory Affairs- Software and Artificial Intelligence (Ultrasound)** The...and all key stakeholders including R&D, Product Management, Quality, Medical & Clinical Affairs, and other functions at all… more
    Philips (07/11/25)
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  • Sr. Regulatory Affairs Specialist - ACM

    Medtronic (Mansfield, MA)
    …This position is most suited for individuals with a broad background covering the total regulatory life cycle of medical devices and strong working knowledge ... and experience with reviewing advertising and promotional materials for medical devices . The initial project scope for this employee will be related to … more
    Medtronic (07/01/25)
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  • Director, US Regulatory Affairs…

    Sanofi Group (Cambridge, MA)
    …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge,...+ Dealt effectively with cross-functional groups, which may include Medical , Legal, Marketing, etc. + Experience managing others is… more
    Sanofi Group (05/22/25)
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  • Regulatory Affairs Specialist - Post Market

    Canon USA & Affiliates (Boston, MA)
    …Good PC skills, including MS Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry required + Minimum ... ** Regulatory Affairs Specialist - Post Market - req1434**...$72,000 to max $116,100 (annual equivalency) **_About us!_** _Canon Medical Systems USA, Inc., a world leader in diagnostic… more
    Canon USA & Affiliates (06/07/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Cambridge, MA)
    …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... to internal regulatory processes and procedures for medical devices and combination products. + Engage...regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory… more
    Sanofi Group (07/15/25)
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  • Principal RA Associate Devices

    Fresenius Medical Center (Waltham, MA)
    …issues and broad design matters. + Understands and interprets US and international medical device regulatory requirements, provides guidance on requirements ... lines. Prepares regulatory submissions required to market new or modified medical devices in the domestic and international clinical markets. Develops and… more
    Fresenius Medical Center (06/14/25)
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  • Program Manager, Regulatory Affairs…

    Olympus Corporation of the Americas (Westborough, MA)
    …Assist the Manager, Regulatory Affairs in obtaining approval to market Olympus medical devices in the markets served by Olympus. **Job Duties** + Facilitate ... **Job Qualifications** **Required:** + Regulatory affairs experience in the Medical Device industry is mandatory. Minimum of 10 years with BS/BA, or 7… more
    Olympus Corporation of the Americas (06/18/25)
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  • Senior Regulatory Affairs Specialist

    Hologic (Marlborough, MA)
    …continuous improvement of regulatory compliance for our capital equipment medical device portfolio. Working cross-functionally with R&D, Quality, Clinical, ... submissions, license renewals, audits, and inspections for capital equipment medical devices + Review and update labeling,...5-8 years' regulatory affairs experience in the medical device industry, ideally with capital equipment… more
    Hologic (07/19/25)
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