• Senior Regulatory Affairs

    West Pharmaceutical Services (Exton, PA)
    Senior Regulatory Affairs Specialist Requisition ID: 71673 Date: Nov 4, 2025 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... and planet through our sustainability efforts. **Job Summary** The Sr. Specialist , Regulatory Affairs , Medical is responsible for influencing department … more
    West Pharmaceutical Services (10/07/25)
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  • Principal Regulatory Affairs

    Philips (New Kensington, PA)
    The Principal Regulatory Affairs Specialist will develop and execute the regulatory strategy for new product development, design changes, and field ... if:** + You've acquired a minimum of 7+ years' experience in Regulatory Affairs /Strategy within FDA regulated Medical Device environments. + You have proven… more
    Philips (11/11/25)
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  • Sr. Specialist Regulatory

    West Pharmaceutical Services (Exton, PA)
    Sr. Specialist Regulatory Affairs , MD Requisition ID: 71773 Date: Nov 21, 2025 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... environment and planet through our sustainability efforts. **Job Summary** The Regulatory Affairs Sr. Specialist is responsible for influencing department … more
    West Pharmaceutical Services (11/14/25)
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  • Sr. Specialist , Regulatory

    West Pharmaceutical Services (Exton, PA)
    Sr. Specialist , Regulatory Affairs , Product Stewardship Requisition ID: 69466 Date: Nov 8, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... and planet through our sustainability efforts. **Job Summary** The Sr. Specialist , Regulatory Affairs evaluates supplier regulatory declarations for… more
    West Pharmaceutical Services (10/10/25)
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  • Principal Regulatory Affairs

    Bausch + Lomb (Harrisburg, PA)
    …with ongoing regulatory training related to products. + Works closely with the Regulatory Affairs labeling group in order to assess and determine the impact ... + Bachelor degree preferred or equivalent + Minimum of 6 years in Regulatory Affairs or relevant experience in a regulated environment + 2+ years of ad/promo… more
    Bausch + Lomb (10/15/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Harrisburg, PA)
    …preferred + Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device, cosmetics ... Strong business acumen and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative ideas to promote a successful … more
    Bausch + Lomb (09/06/25)
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  • Regulatory Specialist C

    University of Pennsylvania (Philadelphia, PA)
    …roles and responsibilities of sponsors, vendors, clinical researchers, and government officials. Regulatory Affairs Specialist C will lead the coordination ... unit research, including but not limited to Phase I-IV clinical trials. The Regulatory Affairs Specialist C will, independently prepare and process all … more
    University of Pennsylvania (10/09/25)
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  • Clinical Research Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …funding. The ACC OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist -CC to participate in the coordination of Phase I-V ... to the Regulatory Affairs Research Teams Manager, the Regulatory Affairs Specialist -CC will, with minimal supervision, prepare and process all … more
    University of Pennsylvania (11/02/25)
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  • Associate Director, Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …train and mentor any reporting Regulatory Affairs Supervisor and/or Regulatory Affairs Specialist A/B/C. In this capacity, the Associate Director ... Summary With the oversight of the Director, the Associate Director for Regulatory Affairs will oversee the portfolio of clinical research undertaken within the… more
    University of Pennsylvania (10/09/25)
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  • Post Market Surveillance Specialist

    Cook Medical (Vandergrift, PA)
    Overview The Regulatory Affairs Specialist - Post Market Surveillance Specialist 2 will be involved in the development and generation of post market ... Follow-Up (PMCF), and Clinical Evaluation Plans and Reports (CEPs, CERs). The Specialist 2 develops regulatory strategies, obtains and maintains approvals, and… more
    Cook Medical (09/16/25)
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