• Terumo Medical Corporation (Somerset, NJ)
    …stakeholders, to include Clinical Affairs , Professional & Clinical Education, Regulatory Affairs , Quality Systems, Marketing, Sales as well as external ... documents and scientific presentations in cooperation with the Clinical, Medical, & Regulatory Affairs Teams, Key Opinion Leaders and physician investigators. +… more
    DirectEmployers Association (10/21/25)
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  • Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the ... could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the… more
    Sanofi Group (10/23/25)
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  • Global Regulatory Affairs CMC…

    Sanofi Group (Morristown, NJ)
    …we chase the miracles of science to improve people's lives. The Global Regulatory Affairs (GRA) CMC & Device Organization within Sanofi R&D serves ... **Job Title:** Global Regulatory Affairs CMC...**Job Title:** Global Regulatory Affairs CMC lead **Location:** Framingham,...GRA CMC Lead within our GRA CMC & GRA Device Organization, you'll drive global regulatory more
    Sanofi Group (10/15/25)
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  • Global Regulatory Affairs CMC…

    Sanofi Group (Morristown, NJ)
    …we chase the miracles of science to improve people's lives. The Global Regulatory Affairs (GRA) CMC & Device Organization within Sanofi R&D serves ... **Job Title:** Global Regulatory Affairs CMC...guidance on Chemistry, Manufacturing, and Controls (CMC) and medical device regulatory requirements across the product lifecycle.… more
    Sanofi Group (10/09/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting ... pathways. The team is accountable for developing and implementing global regulatory strategies for device ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/23/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting ... pathways. The team is accountable for developing and implementing global regulatory strategies for device ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/20/25)
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  • Associate Director, Global

    J&J Family of Companies (Raritan, NJ)
    …Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Regulatory Affairs Diagnostics. This position is a hybrid ... candidates from any location to apply. The Associate Director, Global Regulatory Affairs Diagnostics will...submission of investigational and new in vitro diagnostic medical device applications to the regulatory authorities. This… more
    J&J Family of Companies (10/28/25)
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  • Medical Devices, Regulatory Affairs

    Meta (New York, NY)
    …discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. Experience working ... **Summary:** We're seeking a regulatory affairs specialist to join our...to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.You… more
    Meta (10/08/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …or Madison, New Jersey **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for ... issue resolution, paired with deep expertise in developing and executing global regulatory strategies across drug and device development. + Regulatory more
    Bristol Myers Squibb (10/29/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    …other relevant discipline + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs , with 5+ years specifically within advertising ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion...training and team leadership opportunities. We are an innovative global healthcare company with one purpose: to chase the… more
    Sanofi Group (10/23/25)
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  • Global Medical Affairs Director…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...unmet needs. Sanofi is recruiting a new Director in Global Medical Affairs (GMA) based in Cambridge,… more
    Sanofi Group (10/02/25)
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  • Sr. Manager, Regulatory Affairs Cell…

    ThermoFisher Scientific (Cranbury, NJ)
    …or helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager, Regulatory Affairs , you will play a crucial role in interpreting and ... Day in the Life:** + Interpret and communicate the impact of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical… more
    ThermoFisher Scientific (10/10/25)
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  • Manager, Medical Affairs Strategy

    IQVIA (New York, NY)
    **Manager, Medical Affairs Strategy** **Overview** IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services ... of innovative medical treatments. Our diverse client base includes the global top 20 pharmaceutical, medical device , and biotechnology companies… more
    IQVIA (11/04/25)
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  • Director of Scientific Affairs , COP

    Colgate-Palmolive (New York, NY)
    …York, New York, United States **Who We Are** Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral ... that address a wide range of oral health needs. The Director of Scientific Affairs for Colgate Oral Pharmaceuticals is a pivotal role responsible for leading and… more
    Colgate-Palmolive (10/15/25)
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  • Aesthetics Medical Device & Combination…

    AbbVie (Branchburg, NJ)
    …RDQA) organization, working collaboratively and strategically with colleagues in R&D, Operations, Regulatory Affairs , Medical Safety and more to develop and ... Tik Tok (https://www.tiktok.com/@abbvie) . Job Description As a Medical Device & Combination Product Quality Intern at AbbVie, you...ensure the needs of each site are represented in global procedures. We support the development of a variety… more
    AbbVie (10/08/25)
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  • Global Labeling Lead Specialist

    Kelly Services (Bridgewater, NJ)
    …+ Participate in company audits, as needed **Requirements:** + Knowledge of medical device industry, regulatory affairs , as well as discipline throughout ... Knowledge of standards and regulations relating to submissions and regulatory approval of device products. + Knowledge...Ability to understand and apply business drivers outside of Regulatory Affairs . + Strong communication skills; both… more
    Kelly Services (10/25/25)
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  • Senior Director, Clinical Leader - Neuropsychiatry

    J&J Family of Companies (Titusville, NJ)
    …via matrix interactions also includes individuals from project management, TA strategy, global regulatory affairs , finance, legal, quality assurance, quality ... for the preparation and approval of essential documents for global regulatory filings. The CL will manage...Team and its affiliates + Assists Regulatory Affairs in the development of drug/ device more
    J&J Family of Companies (11/05/25)
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  • Director, Study Responsible Physician - Mivexian

    J&J Family of Companies (Raritan, NJ)
    …for worldwide health authorities concerning clinical/medical issues + Assists Regulatory Affairs in the development of drug/ device regulatory strategies ... 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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  • Director, Inspection Readiness

    Bristol Myers Squibb (New Brunswick, NJ)
    …in pharmaceutical (medical device , biologics) facilities. + In-depth knowledge of global regulatory requirements (FDA, EMA, PMDA, etc.) and GxP standards. + ... agency inspections (eg, FDA, EMA, PMDA, etc.) across global pharmaceutical, biotech, cell therapy, and medical device...fields, required. + 10+ years of relevant experience in regulatory affairs , compliance, or quality assurance in… more
    Bristol Myers Squibb (10/30/25)
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  • Sr Medical Science Liaison, Selution (Northeast…

    Cordis (New York, NY)
    …of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart ... treatments for coronary and peripheral artery diseases. With four Investigational Device Exemptions (IDEs) approved and actively enrolling patients (Coronary ISR,… more
    Cordis (10/21/25)
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