• Medical Devices , Regulatory

    Meta (New York, NY)
    …a scientific discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. ... regulatory affairs specialist to join our medical devices compliance team. You will get...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
    Meta (10/08/25)
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  • Co-Op: Regulatory Affairs (12…

    Haleon (Warren, NJ)
    …legislation covering pharmaceuticals, medical devices , cosmetics and foods. The Regulatory Affairs team helps to guide our company on our responsibility ... us achieve this goal. Right now, we're looking for a Co-Op student in US Regulatory Affairs to join us to do career defining work. **A career in Regulatory more
    Haleon (09/10/25)
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  • Staff Regulatory Affairs Specialist

    embecta (Parsippany, NJ)
    …discipline (eg engineering, bioengineering, biology, chemistry). + 5+ years Regulatory Affairs experience in medical device companies. + Must have ... in both the US and Europe, and related regulatory affairs activities to ensure compliance with...current knowledge of the US and European Medical Device regulations. + Demonstrated success in… more
    embecta (10/07/25)
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  • Aesthetics Medical Device

    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...procedures. We support the development of a variety of medical devices in the Aesthetics space, including… more
    AbbVie (10/08/25)
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  • Project Manager, Scientific Operations

    Kelly Services (Raritan, NJ)
    …Supports creation of project value propositions as needed. + Provides strong connectivity with Medical Affairs , R&D, Regulatory Affairs , and Clinical ... communication skills across different organization levels **Preferred:** + Prior experience in medical devices or other regulated industry + Knowledge of… more
    Kelly Services (09/30/25)
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  • Global Regulatory Affairs CMC lead

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

    Sanofi Group (Morristown, NJ)
    …(3+ years preferred) of regulatory experience, preferably within the pharmaceutical/ medical device /biotech industry + Knowledge and understanding of complex ... **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location**...R&D colleagues, as well as other stakeholders (eg, Legal, Medical , Marketing, Communications and Compliance). + Participates in the… more
    Sanofi Group (09/30/25)
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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 ... miracles of science to improve people's lives", Specialty Care Medical Affairs have a vision to be...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs more
    Sanofi Group (10/02/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …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...cross-functional teams + Develop and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/23/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... team is part of the Global Regulatory Affairs , Regulatory CMC and Device ...to internal regulatory processes and procedures for medical devices and combination products. + Engage… more
    Sanofi Group (07/15/25)
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  • GRA Device Lead (Associate Director)

    Sanofi Group (Morristown, NJ)
    …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...cross-functional teams. + Develop and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/20/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …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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  • Sr Medical Science Liaison

    Terumo Medical Corporation (Somerset, NJ)
    …product and scientific support for the organization that includes Medical Affairs , Clinical Operations, Sales, Marketing, Regulatory Affairs , to ensure ... therapeutic area, provide support in the following ways: + Medical affairs strategy: + Contribute to the...+ Regulatory activities partnership: + Work with regulatory affairs to ensure that all written… more
    Terumo Medical Corporation (10/01/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (Manhattan, NY)
    regulatory strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides ... staff + May have responsibility for maintaining a compliant medical device quality system for R&D and...years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the… more
    Grifols Shared Services North America, Inc (10/03/25)
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  • Director, Data Science (RWE & GenAI), Diagnostics…

    Danaher Corporation (New York, NY)
    regulatory , market access, and post-market). You'll collaborate with clinical, regulatory /quality, R&D, medical affairs , IT/security, and our Operating ... and visualization tools. + Proven experience analyzing RWE/RWD (EHR, claims, registries, device logs) for clinical, regulatory , or market access impact. Travel,… more
    Danaher Corporation (10/03/25)
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  • Director, Regulatory Policy & Intelligence

    Organon & Co. (Jersey City, NJ)
    …Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and products, as well as ... of the world of interest to Organon. **Responsibilities** + Provide Global Regulatory Policy and Intelligence insights to the organization to guide product… more
    Organon & Co. (07/23/25)
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  • Regulatory Coordinator

    Insight Global (New York, NY)
    …Skills and Requirements -2+ years of experience working in regulatory affairs (especially product registration) -Experience within cosmetic, ... large CPG client of ours is looking for a regulatory coordinator for a 5 month (starting) contract that...CPG, pharma, or medical device industries -BS Degree in Scientific… more
    Insight Global (10/03/25)
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  • Manager, Contract Management Cardiopulmonary (CP)…

    J&J Family of Companies (Raritan, NJ)
    …TA (TA R&D BD liaison for biology, Clinical Development) and partnering functions ( Regulatory , Global Development, Medical Affairs , Commercial). + Share ... of 5 years' experience working in the global Pharmaceutical, Biotechnology or Medical Device /Diagnostics industry or an institution that participates in… more
    J&J Family of Companies (09/26/25)
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  • Sr Medical Science Liaison, Selution…

    Cordis (New York, NY)
    …key clinical and scientific insights to internal stakeholders-such as Clinical Development, Medical Affairs , and Commercial teams, helping shape strategy and ... and medical information between KOLs, other investigators and the company's Medical Affairs , Marketing and R&D groups. + Propose strategic solutions to… more
    Cordis (07/22/25)
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  • Subchapter Lead Companion Diagnsotics

    Roche (Branchburg, NJ)
    …with expertise in Companion Diagnostics. + Knowledge in IVD, Pharmaceutical, and /or Medical Device industry; Regulatory Compliance, Federal cGMP's and ... ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to...you will be a member of the companion diagnostics Regulatory Affairs Leadership team. In this position,… more
    Roche (09/26/25)
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