• Exec Director, Regulatory Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    …directly relevant professional experience in small molecule and biologics development, global CMC regulatory affairs and CMC technical areas of at least 16 years ... PhD, PharmD, or MD. + Demonstrated track record in leading CMC regulatory affairs initiatives, innovative CMC regulatory strategies, and leadership in… more
    Gilead Sciences, Inc. (08/08/25)
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  • Regulatory Affairs Assoc II CMC…

    Gilead Sciences, Inc. (Foster City, CA)
    …Join Gilead and help create possible, together. **Job Description** This exciting role of Regulatory Affairs Associate II, CMC sits in Gilead's CMC Regulatory ... are as follows: **Responsibilities:** + Provides support for designated regional regulatory activities for PDM CMC Project and Commercial Teams, Regulatory more
    Gilead Sciences, Inc. (07/29/25)
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  • Manager, Rates and Regulatory

    Liberty Utilities (Downey, CA)
    Manager, Rates and Regulatory Affairs Litchfield Park, AZ, US, 85340Downey, CA, US, 90241 **Our purpose is sustaining energy and water for life, and it is ... utilities in the West region. This position is responsible for all regulatory affairs and rates related functions in multiple jurisdictions. The Manager will… more
    Liberty Utilities (07/08/25)
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  • Director, Regulatory Affairs CMC

    Gilead Sciences, Inc. (Foster City, CA)
    …guidance. + Collaborates with colleagues across the global CMC RA organization, Gilead Regulatory Affairs , and affiliates on internal meetings and leads global ... system. **Qualifications** + Bachelor's degree and 12+ years of experience in CMC Regulatory Affairs (CMC RA) or other relevant industry experience or 10 + years… more
    Gilead Sciences, Inc. (06/27/25)
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  • Regulatory Affairs Manager…

    Abbott (Alameda, CA)
    …their glucose levels with our new sensing technology. **The Opportunity** This ** Regulatory Affairs Manager - International Compliance Operations** will work ... people monitor their glucose levels with our new sensing technology. This ** Regulatory Affairs Manager - International Compliance Operations** will provide… more
    Abbott (06/21/25)
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  • Regulatory Affairs Specialist II…

    Abbott (Santa Clara, CA)
    …place to work for diversity, working mothers, female executives, and scientists This ** Regulatory Affairs Specialist II** will work on-site at our Santa Clara, ... + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a...in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a plus. Apply Now… more
    Abbott (05/17/25)
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  • Staff Regulatory Affairs Specialist,…

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …+ RAPS RAC certification preferred + Minimum of 5 years of strong Regulatory Affairs /Compliance experience in medical devices + Experience with end-to-end SaMD ... (including all documents required under risk files). + Knowledge of global Regulatory Affairs requirements, regulations, and standards + Strong prioritizing,… more
    BD (Becton, Dickinson and Company) (06/27/25)
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  • Principal Regulatory Affairs

    Abbott (Alameda, CA)
    …years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. . Experience with ... the spectrum of customer needs. Projects will focus on driving the regulatory strategy for business partnership initiatives involving Cloud/ Sensor based external… more
    Abbott (07/22/25)
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  • Principal Regulatory Affairs

    Abbott (Alameda, CA)
    …years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. + Experience with ... monitor and influence changing regulations and guidance, interface with outside regulatory agencies and trade associations, develop innovative regulatory more
    Abbott (06/28/25)
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  • Senior Manager, Global Regulatory

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
    Otsuka America Pharmaceutical Inc. (06/19/25)
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