• Sr . Regulatory Affairs

    Teleflex (Wyomissing, PA)
    Sr . Regulatory Affairs Associate **Date:** Dec 23, 2025 **Location:** Wyomissing, PA, US **Company:** Teleflex **Expected Travel** : None **Requisition ... in patients' lives. **Position Summary** The Sr Regulatory Affairs (RA) Associate will...quality system compliance requirements. The Senior RA Associate will partner with Product Management Regulatory more
    Teleflex (11/24/25)
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  • Senior Regulatory Affairs

    Parexel (Nashville, TN)
    …FDA regulatory requirements and processes to a major, dedicated client partnership. As a Senior Regulatory Affairs Associate , you will serve as the ... and guidelines to Parexel! We are currently seeking a highly motivated Regulatory Affairs professional to join Parexel and contribute their knowledge of… more
    Parexel (12/20/25)
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  • Regulatory Affairs Associate

    GRAIL (Albany, NY)
    …products with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and leadership. They may manage and provide direction to regulatory staff and, when required, participate in senior...of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties… more
    GRAIL (12/03/25)
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  • Associate Director, Regulatory

    University of Pennsylvania (Philadelphia, PA)
    Regulatory Job Description Summary With the oversight of the Director, the Associate Director for Regulatory Affairs will oversee the portfolio of ... clinical research undertaken within the department/division. The Associate Director for Regulatory Affairs assists the Director in providing direction and… more
    University of Pennsylvania (01/07/26)
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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 ... We invite candidates from any location to apply. The Associate Director, Global Regulatory Affairs ...to present complex information to cross-functional project teams and senior management in a clear and concise manner is… more
    J&J Family of Companies (01/07/26)
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  • Associate Director, Global…

    Takeda Pharmaceuticals (Cambridge, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA ... medicine promotion. **How you will contribute:** + As our Associate Director, Global Regulatory Affairs ...if there is new data or campaigns that require senior level management input or alignment. + Strategic business… more
    Takeda Pharmaceuticals (10/29/25)
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  • Sr . Manager, Payor Relations…

    Abbott (Livermore, CA)
    …their lives. This position leads payor relations (including payor contracting) and regulatory affairs , which are foundational functions to driving ongoing ... major US-based health plans, in accordance with corporate policies and regulatory requirements + Leads organization through all activities required to maintain… more
    Abbott (12/20/25)
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  • Assistant Director Government Relations

    Penn Medicine (Philadelphia, PA)
    …and Delaware. Reporting to the Senior Director of Government Relations and Regulatory Affairs , the Associate Director helps develop and implement Penn ... the Senior Director of Government Relations and Regulatory Affairs on strategic initiatives and short-... strategy that aligns with organizational goals, including the Associate Vice President of Government and Community Relations and… more
    Penn Medicine (12/24/25)
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  • Regulatory Writing Sr Mgr

    Amgen (Washington, DC)
    …12 years of directly related experience **Preferred Qualifications:** + Experience with regulatory documents in Regulatory Affairs , Research, Development or ... time for a career you can be proud of. ** Regulatory Writing Senior Manager** **Live** **What you...degree and 8 years of directly related experience OR Associate 's degree and 10 years of directly related experience… more
    Amgen (12/18/25)
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  • Program & Technical Advisor ( Sr

    Guidehouse (Mclean, VA)
    …FDA/ICH guidelines and CDISC data standards + Experience in pharmaceutical industry regulatory affairs and/or quality assurance and/or quality control + Direct ... research and technical evaluation panels. You'll also advise on clinical, regulatory , and manufacturing aspects of medical product development, ensuring alignment… more
    Guidehouse (11/09/25)
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