• Senior Manager, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Durham, NC)
    …Requirements:** + **Experience:** Minimum of 8 years of directly related Regulatory Affairs experience in medical devices and/or in vitro diagnostic ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...possible** with us. **Position Summary** The Senior Manager of Regulatory Affairs reports directly to the Senior… more
    BD (Becton, Dickinson and Company) (10/30/25)
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  • Clinical Research Leader - JJMT Neurovascular

    J&J Family of Companies (Irvine, CA)
    …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... study team; o Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality/ Regulatory , Medical Affairs , Medical Safety) to… more
    J&J Family of Companies (11/01/25)
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  • Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    …teams + Develop and execute innovative and sustainable medical device regulatory strategies covering stand-alone medical devices and device part ... **Job title** : Global Regulatory Affairs Device Lead...to internal regulatory processes and procedures for medical devices + Accountable for regulatory more
    Sanofi Group (10/23/25)
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  • Clinical Research Manager - JJMT Electrophysiology

    J&J Family of Companies (Irvine, CA)
    …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... based on study need; + In EMEA, responsible for Regulatory Affairs related tasks associated with clinical...with budget planning, tracking and control is required. + Medical Device experience is required. + Sound… more
    J&J Family of Companies (09/12/25)
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  • Medical Director, Medical

    AbbVie (North Chicago, IL)
    …in close collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs , medical writing, clinical development, clinical ... to other AbbVie office locations in the US. Purpose: Medical Device Safety Physician leads the safety...documented prior to submission of reports, including MDRs, to regulatory authorities. + Provide medical input and… more
    AbbVie (10/26/25)
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  • Director, Study Responsible Physician - Mivexian

    J&J Family of Companies (Raritan, NJ)
    …health authorities concerning clinical/ medical issues + Assists Regulatory Affairs in the development of drug/ device regulatory strategies + ... via matrix interactions also includes individuals from project management, operations, regulatory affairs , data management, medical writing, biostatistics,… more
    J&J Family of Companies (10/23/25)
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  • Principal Research Scientist I, Tissue Material…

    AbbVie (Irvine, CA)
    …to be a team leader and engage key stakeholders, including global strategic marketing, medical affairs , regulatory affairs , clinical development, and ... be to evaluate the interaction of current and future medical devices with cells and tissues for...methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory more
    AbbVie (09/23/25)
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  • Director, Regulatory Affairs

    BeOne Medicines (Emeryville, CA)
    **General** **Description:** The Director, Regulatory Affairs , Dx/CDx and Medical Devices will be responsible for leading a small team for developing and ... implementing regulatory diagnostic and medical device ...externally with a solid background in medical devices /diagnostic development regulations and associated regulatory deliverables.… more
    BeOne Medicines (10/12/25)
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  • Medical Device & Combo Product…

    AbbVie (North Chicago, IL)
    …RDQA) organization, working collaboratively and strategically with colleagues in R&D, Operations, Regulatory Affairs , Medical Safety and more to develop ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description As a Medical Device & Combination Product Quality Knowledge Management Intern at… more
    AbbVie (10/09/25)
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  • Senior Manager, Regulatory Affairs

    Dentsply Sirona (Sarasota, FL)
    …**Years and Type of Experience:** + 8(+) years of experience in regulatory affairs , preferably in the medical device industry + Experience with leading ... implements regulatory strategies to obtain and maintain regulatory approvals for medical devices ...+ Experience with software as a medical device , AI and/or medical devices more
    Dentsply Sirona (11/20/25)
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