• Senior Principal Regulatory Affairs…

    Bausch + Lomb (Madison, WI)
    …degree or equivalent; Master's degree preferred + Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, ... US and/or Canada + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical /non- clinical...and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative… more
    Bausch + Lomb (09/06/25)
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  • Director, Regulatory Affairs

    BeOne Medicines (San Mateo, CA)
    **General Description:** The Director, Regulatory Affairs will be responsible for developing, implementing, and advising on North America (NA) regulatory ... mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical...candidates will have experience working as a lead in Regulatory Affairs with the FDA and prior… more
    BeOne Medicines (09/06/25)
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  • Regulatory Affairs Associate

    Envista Holdings Corporation (Brea, CA)
    **Job Description:** The ** Regulatory Affairs Associate** (RAA) supports the RA team in creating, evaluating and completing regulatory tasks related to ... (BA/BS) from four-year college/university plus 1+ year experience in regulatory affairs **or** Master's Degree in ...take that approach when we help orthodontists achieve their clinical and practice management objectives. We take the same… more
    Envista Holdings Corporation (08/08/25)
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  • Associate Director, Global Regulatory…

    Organon & Co. (Jersey City, NJ)
    …Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and outside. + Communicate new legislations, guidelines and ... entire life cycle of the drug. + Represent Global Regulatory Affairs within our company's internal committees...complexity level, as well as post-approval products with limited clinical development + Regulatory product and compliance… more
    Organon & Co. (07/26/25)
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  • Associate Director, Global Regulatory…

    Takeda Pharmaceuticals (Boston, MA)
    …Proactively recognizes and contributes to enhancing business processes. As part of the Global Regulatory Affairs CMC team, you will report to the Senior Director ... Regulatory , Pharmaceutical Development, and Production project teams throughout clinical development and commercial lifecycle for assigned products and...Global Regulatory Affairs CMC. **How you will contribute:**… more
    Takeda Pharmaceuticals (07/08/25)
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  • Clinical Affairs Manager,…

    Teleflex (Wayne, PA)
    Clinical Affairs Manager, Interventional Access, EAST REGION (REMOTE) **Date:** Aug 11, 2025 **Location:** Wayne, PA, US **Company:** Teleflex **Expected ... make a difference in patients' lives. **Position Summary** The Clinical Affairs Manager will provide clinical...expertise, insight, and support to clinical end-users, clinical sales specialists, sales team, Regulatory , Engineering,… more
    Teleflex (08/13/25)
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  • Director, Global Regulatory Affairs

    Candela Corporation (Marlborough, MA)
    **Director, Global Regulatory Affairs ** Requisition Number **2872** Location **US - Marlborough, MA** State/Territory **Massachusetts** **Company Overview:** ... and audit/inspection readiness. + Global accountability to establish/maintain a high-performance Regulatory Affairs team. + Actively support New Product… more
    Candela Corporation (08/29/25)
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  • Director, QA Regulatory Affairs

    Fujifilm (Research Triangle Park, NC)
    **Position Overview** The Director, QA Regulatory Affairs is a pivotal role providing regulatory expertise and leadership to the FUJIFILM Biotechnologies ... Description** **What You'll Do** + Leads, mentors, and sets the objectives for the Regulatory Affairs team across the North Carolina sites + Performs … more
    Fujifilm (08/27/25)
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  • Associate Director, Regulatory…

    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 ... Advanced degree preferred; 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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  • Senior Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist** to join our team on-site in Plymouth, ... MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory guidance… more
    Abbott (08/18/25)
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