• Principal Device Development

    Regeneron Pharmaceuticals (East Greenbush, NY)
    …+ Or equivalent combination of education and experience Previous experience in combination product/ medical device development or similar area is required. ... Regeneron is currently looking for a Principal/Staff Device Development Engineer to join our...an off the shelf, or an internally designed platform medical device delivery system. + Defines detailed… more
    Regeneron Pharmaceuticals (06/11/25)
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  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …with a track record of handling multiple programs and streams of work. + Experience with medical device development standards eg ISO 13485, FDA 21 CFR 820 + ... production and align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management,… more
    US Tech Solutions (07/18/25)
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  • Executive Director, Clinical Development

    Bausch Health (Bothell, WA)
    …drive our collective progress and impact. We are seeking an Executive Director, Clinical Development for our Medical Device Aesthetics business (Solta) to be ... position provides a unique opportunity to drive innovation through the development of new medical device technologies and applications in a fast-paced R&D… more
    Bausch Health (06/28/25)
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  • Associate Director - Device

    Lilly (Indianapolis, IN)
    …**Minimum Requirements:** + 5+ years of experience in asset/project delivery and/or medical device development & commercialization + Demonstrated Project ... will provide leadership for Commercialization Global Program Managers (GPM's) who lead medical device and drug/ device combination product commercialization… more
    Lilly (08/27/25)
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  • Quality Engineer (Electromechanical Medical

    AbbVie (Pleasanton, CA)
    …(QSR), ISO 13485, ISO 14971, MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & + ... Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year… more
    AbbVie (06/26/25)
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  • Senior Project Manager - Medical

    ICS (Waltham, MA)
    …SummaryWe are seeking a seasoned Senior Project Manager with extensive experience in the medical device software development sector. In this critical role, ... Senior Project Manager - Medical Device Software Waltham, MA Apply...of progressive experience in project management within a software development environment. + 3-5 years of direct experience managing… more
    ICS (07/26/25)
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  • System Integration Engineer - Medical

    Philips (Bothell, WA)
    …Systems Engineering and product integration and testing in FDA Regulated (ISO 13485) Medical Device product development (other highly regulated environments ... **System Integration Engineer - Medical Device Hardware (Bothell, WA)** You... Hardware (Bothell, WA)** You will contribute to the development and release of best-in-class Ultrasound innovations influencing the… more
    Philips (08/20/25)
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  • Cyber Security Specialist, Medical

    Community Health Systems (Franklin, TN)
    …+ Proactive identification and solving of complex problems + Strong understanding of medical device and IOMT system development to provide technical ... **Job Summary** As a Medical Device and IoMT Security Specialist, this role reports to the Manager of Endpoint Security. This role develops, engineers, and… more
    Community Health Systems (08/29/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …projects. The incumbent will work closely with key stakeholders including clinical, medical affairs, Industrial Affairs ( Device Development , manufacturing, ... team is a globally diverse team supporting the medical device , combination product, digital health and...part of the Global Regulatory Affairs, Regulatory CMC and Device Department within Global Research and Development .… more
    Sanofi Group (07/15/25)
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  • Associate Engineering Fellow, Combination Product…

    Takeda Pharmaceuticals (Lexington, MA)
    …13+ years or PhD and 7+ years preferably within the biopharmaceutical industry or medical device development and commercialization are desired. + Minimum of ... + Support the optimization of design control elements to comply with combination produce/ medical device regulations. Lead or assist in deviation, complaint and… more
    Takeda Pharmaceuticals (08/20/25)
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