• Associate Director, Regulatory Affairs

    United Therapeutics (Sacramento, CA)
    …of biologic or pharma regulatory experience with a Bachelor's Degree in life sciences, quality , regulatory affairs or a related area of study or 10+ years of ... biologic or pharma regulatory experience with a Master's Degree in life sciences, quality , regulatory affairs or a related area of study or 7+ years of… more
    United Therapeutics (08/07/25)
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  • Regulatory Affairs Manager

    Alameda Health System (Oakland, CA)
    … or patient care experience; two years in accreditation/licensing/ regulatory compliance/ quality /performance improvement/patient safety in healthcare; ... Regulatory Affairs Manager + oakland, CA + Quality + Regulatory Affairs + Full Time...and compliant investigations. 5. Identifies growth and areas of opportunity to enhance Regulatory Affairs and AHS… more
    Alameda Health System (08/09/25)
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  • SCI Senior Regulatory Specialist (Hybrid)

    Stanford University (Stanford, CA)
    …communication skills, teamwork, and superb attention to detail. We strive for top- quality regulatory support of investigator-initiated clinical trials with a ... SCI Senior Regulatory Specialist (Hybrid) **School of Medicine, Stanford, California,...continuous improvement. **Duties include*:** + Lead the planning and operations for programs or functions that have significant business,… more
    Stanford University (08/07/25)
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  • Principal Regulatory Affairs Specialist…

    Medtronic (Santa Rosa, CA)
    …and influences the preparation of documentation to support innovative and high- quality regulatory submissions from early phase strategies, marketing ... to engineer the extraordinary. Join a diverse team of Regulatory Affairs Professionals who bring their knowledge, their unique...is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color,… more
    Medtronic (07/25/25)
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  • Senior Director, Corporate & Regulatory

    Edwards Lifesciences (Irvine, CA)
    …Edwards. Providing exceptional legal guidance on the Company and TAVR business's commercial, regulatory , clinical and quality legal issues, this role will also ... with the utmost diligence and care. You'll have the opportunity to work with a dedicated team and build...support to Edwards' leaders on medical device commercial, clinical, regulatory , quality and reimbursement related legal matters,… more
    Edwards Lifesciences (06/12/25)
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  • Staff Specialist Regulatory Affairs…

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …for SaMD products, including evaluation of cybersecurity risks. + Collaborate with R&D, Quality , Marketing, and Regulatory teams to ensure regulatory ... **Job Description Summary** As Staff Specialist Regulatory Affairs, you will have a deep understanding...compliance, expedition of product clearances and maintain the highest quality standards. Candidates will be expected to work on-site… more
    BD (Becton, Dickinson and Company) (05/22/25)
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  • Associate Director, Global TA Regulatory

    Gilead Sciences, Inc. (Foster City, CA)
    …relevant experience. + BA/BS with 10+ years' relevant experience. + Significant regulatory , quality , compliance or related experience in the biopharma industry. ... create possible, together. **Job Description** You will act as the Regional Regulatory Lead on more complex or multiple products, compounds, indications or projects… more
    Gilead Sciences, Inc. (08/02/25)
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  • Director of Product Quality

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …Field Action decision, as applicable. + Collaborates with leadership in Business Unit Quality , Regulatory Affairs, R&D, Operations , Service, Medical Affairs, ... field + Minimum of 10 years of experience in Quality or Regulatory function within the medical...Quality function requiring technical product expertise (Design Assurance, Quality Operations , etc.) + Experience in full… more
    BD (Becton, Dickinson and Company) (07/18/25)
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  • Principal Quality Mfg Engineer, Selution

    Cordis (Irvine, CA)
    … and manufacturing process, as well as responsible for overseeing and managing operations quality programs, initiatives and guiding the operations team ... every stage of the manufacturing process, ensuring compliance with regulatory standards and internal quality requirements. +...regulations. + MDR: Primary point of contact for the quality operations team for MDR, with potential… more
    Cordis (05/15/25)
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  • Principal Supplier Quality Engineer,…

    Cordis (Irvine, CA)
    regulatory requirements. + Provide guidance to suppliers on quality expectations and compliance improvements. + **Cross-Functional Collaboration** + Work closely ... are the people behind the people who keep saving lives.** The **Principal Supplier Quality Engineer (SQE)** will be responsible for ensuring the quality and… more
    Cordis (07/29/25)
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