• AD / Dir Regulatory Affairs Strategy

    System One (Florham Park, NJ)
    Job Title: AD or Director, Regulatory Affairs Strategy Location: Florham Park, NJ (10 days onsite per month) Type: 12-month contract Must haves: + Must be local for ... development, not just life cycle management. Overview Support the Regulatory Affairs (Executive Director) in developing and executing regulatory strategies for… more
    System One (08/20/25)
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  • Regulatory Affairs & Safety Associate, HH

    Reckitt (Parsippany, NJ)
    Regulatory Affairs & Safety Associate, HH City: Parsippany **We...pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in ... to grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate, Regulatory and Compliance provides regulatory and compliance support… more
    Reckitt (08/21/25)
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  • Associate Director, Regulatory Affairs

    Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
    Associate Director, Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... with at least 10+ years- experience in a regulatory affairs . + Primary experience must be managing a significant...Use various labeling software tools such as TVT and/or Global Vision. Can be trained and have direct reports… more
    Glenmark Pharmaceuticals Inc., USA (08/15/25)
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  • Senior Director, Managed Access Programs, Medical…

    Bristol Myers Squibb (Madison, NJ)
    …be responsible for partnering to develop the strategy and lead the global implementation and management of Managed Access Programs across multiple disease areas. ... : Serve as the primary point of contact for internal (Medical Affairs , Development, Commercial, Regulatory Affairs , Legal, and Compliance) and external… more
    Bristol Myers Squibb (08/13/25)
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  • Senior Manager, Regulatory Affairs - OTC

    Haleon (Warren, NJ)
    …everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, ... part of something special. **About the role** This **Senior Manager, Regulatory Affairs - OTC** has responsibility for end-to-end regulatory activities for the OTC… more
    Haleon (09/03/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge, MA or Morristown, NJ **About the job** Are you ready to shape the ... could be critical in helping our teams accelerate progress. We are an innovative global healthcare company with one purpose: to chase the miracles of science to… more
    Sanofi Group (08/08/25)
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  • Associate Director, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    **Job Description Summary** As Associate Director, Regulatory Affairs , you will be responsible for leading RA team members involved in device project activities and ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...medical training preferred. + Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries,… more
    BD (Becton, Dickinson and Company) (08/27/25)
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  • Associate Principal Scientist, Regulatory…

    Organon & Co. (Jersey City, NJ)
    …for assigned small molecule and/or biological products in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist ... products through the product lifecycle. + Lead development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of CMC… more
    Organon & Co. (07/22/25)
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  • Associate Director, Statistics - (Hybrid)

    AbbVie (Florham Park, NJ)
    …projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Associate Director works in partnership with ... experts in multiple disciplines to advance medicines to our patients. Responsibilities: + Provide expertise/lead regulatory submission and product life-cycle management strategy planning and implementation for assigned projects. Provide statistical leadership… more
    AbbVie (08/30/25)
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  • Manager, Statistics

    AbbVie (Florham Park, NJ)
    …organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Manager works independently in partnership with ... experts in multiple disciplines to advance medicines to our patients. Responsibilities: + Provide expertise to design, analysis and reporting of clinical trials or other scientific research studies. Independently develop protocols and/or statistical analysis… more
    AbbVie (07/24/25)
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