• Medical Device Regulatory Affairs

    Abbott (Santa Clara, CA)
    …and scientists. **The Opportunity** We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) Program** to be located ... Abbott is a global healthcare leader that helps people live more...of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000… more
    Abbott (09/06/25)
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  • Winter-Spring 2026 Co-op-Intern - Public…

    Sanofi Group (Cambridge, MA)
    **Job Title** : Winter-Spring 2026 Co-op-Intern - Public Affairs and Patient Advocacy **Location:** Cambridge, MA **About the Job** Looking to launch your career at ... people worldwide. **As** **a** **Winter/Spring 2026 Co-op/Intern - Public Affairs and Patient Advocacy** , you'll spend your time...the best in the industry. We are an innovative global healthcare company, committed to transforming the lives of… more
    Sanofi Group (07/23/25)
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  • Associate Director, Commercial Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Provides regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical Affairs , Public Affairs , Value Access and Payment, and ... and maintain strong working relationships with internal customers, including Commercial, Medical , Public Affairs , Legal and Compliance + Integrate compliance… more
    Bristol Myers Squibb (09/14/25)
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  • Senior Project Manager, Cell Therapy…

    Bristol Myers Squibb (Princeton, NJ)
    …leads matrixed cross-functional project management teams and projects within the Medical Affairs Cell Therapy Organization. This role reports directly ... Medical organization to deliver key portfolio priorities. Responsibilities include global and regional brand and medical planning, budget planning, congress… more
    Bristol Myers Squibb (08/28/25)
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  • Program Manager, Regulatory Affairs

    GE HealthCare (Chicago, IL)
    …the factors that differentiate them in the market. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create ... compliance, working closely with healthcare regulatory bodies globally. + Prepares global regulatory submissions by working across the regulatory organization and… more
    GE HealthCare (06/25/25)
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  • Manager, Regulatory Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    …Specific Education & Experience Requirements: + 5+ years of experience in Regulatory Affairs or other relevant industry experience. + Degree in a scientific field is ... submissions which require interactions with departments outside of Regulatory Affairs for investigational and commercial products for assigned territories in… more
    Gilead Sciences, Inc. (09/06/25)
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  • Senior Director, Regulatory Affairs - CMC

    Bristol Myers Squibb (Indianapolis, IN)
    …by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals . We are seeking an experienced and motivated ... **Senior Director, Regulatory Affairs - CMC (Manufacturing)** . This position will report...(MAA) submissions + Lead the development and execution of global CMC regulatory strategies for activities conducted at the… more
    Bristol Myers Squibb (09/14/25)
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  • Medical Affairs Associate Director

    IQVIA (Durham, NC)
    …role but may require onsite visits to clients. **Role and responsibilities** + Represent Medical Affairs on the content review committee as the lead Medical ... **Job Description** IQVIA Pharma Review provides outsourced medical copy review and approval services and advisory...Promomats and/ or Aprimo desorable IQVIA is a leading global provider of clinical research services, commercial insights and… more
    IQVIA (08/12/25)
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  • Quality Assurance & Regulatory Affairs

    Catalent Pharma Solutions (St. Petersburg, FL)
    **Quality Assurance & Regulatory Affairs Compliance Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing ... and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments… more
    Catalent Pharma Solutions (08/19/25)
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  • Vice President, Spine Regulatory Affairs

    IQVIA (Washington, DC)
    …discipline; MS or PhD preferred.** **Minimum fifteen years of experience in Regulatory Affairs related to development of medical devices, drugs and/or biologics, ... Overview** **MCRA, an IQVIA business is seeking a Vice President, Spine Regulatory Affairs to be a critical team member and Company leader supporting regulatory… more
    IQVIA (09/11/25)
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