• Advisor, Clinical Research

    Abbott (Santa Clara, CA)
    …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well as ... live a full life. You'll also have access to: + Career development with an international company where you can grow the career you dream of. + Employees can qualify… more
    Abbott (05/28/25)
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  • Senior Counsel

    Fujifilm (Sacramento, CA)
    …Secretary, the Senior Counsel, will be responsible for handling all legal affairs relating to the ink and chemicals manufacturing businesses and the corporate ... https://www.fujifilm.com/us/en/about/region/careers **Job Description** **Responsibilities** + Advise on day-to-day legal affairs , various domestic and cross-border transactions, contracts, compliance, and… more
    Fujifilm (05/14/25)
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  • Associate Director, Medical Events Group

    Abbott (Alameda, CA)
    …Minimum of 5 years of experience in Quality Systems, Quality Assurance and/or Regulatory Affairs + Medical device industry or other regulated environment ... also have access to: + Career development with an international company where you can grow the career you...Function as a representative during audits, inspections, assessments by regulatory agencies, eg FDA for the medical event reporting… more
    Abbott (05/23/25)
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  • Labeling Specialist II

    Abbott (Sylmar, CA)
    …medical device products. Coordinates with Engineering, Marketing, Clinical Research, and Regulatory Affairs to define product labeling requirements. Designs and ... and IFUs from Engineering (Manufacturing, Packaging, etc.), Marketing, Clinical Research, and Regulatory Affairs (RA) to define specific requirements for product… more
    Abbott (06/10/25)
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  • Vice President, Product Innovation Management,…

    Danaher Corporation (Sunnyvale, CA)
    …(NPD) core teams to execute on. + Partner with R&D and Clinical & Regulatory Affairs to drive innovation execution by fostering Product Innovation Manager ... key stakeholders across the organization, including R&D, Clinical & Regulatory Affairs , and Marketing. + Lead a...travel of up to 30% and may include some international travel. + Must be able to sit for… more
    Danaher Corporation (04/29/25)
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  • Design Quality Engineer I

    Actalent (Irvine, CA)
    …collaboration skills with departments like Advanced Operations, Product Development, Regulatory Affairs , and Marketing. + Strong interpersonal, written, ... holidays, and standard benefits. The role requires interaction with regulatory agencies and adherence to US and International... regulatory agencies and adherence to US and International Medical Device Regulations. Pay and Benefits The pay… more
    Actalent (06/07/25)
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  • Senior Manager, Early-stage Biologics Development,…

    Vera Therapeutics (Brisbane, CA)
    …including Research, Clinical Pharm, Analytical Science, Drug product, Quality Assurance, Regulatory Affairs , Supply chain, Finance, and Program Management. Write ... team and other functions such as Research, QA, and Regulatory , the ideal candidate must be an outstanding leader...and protein production) is required. * Experience in managing US/ international CDMOs for the manufacture of non-GMP and cGMP… more
    Vera Therapeutics (04/09/25)
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  • Principal Engineer, Device Development

    AbbVie (Irvine, CA)
    …software, electrical, and systems engineering teams, as well as quality assurance and regulatory affairs , to ensure seamless product integration. + Stay abreast ... also involve interactions with CMC drug products, analytical efforts, regulatory requirements, quality standards, operations, external customers, users, contract… more
    AbbVie (06/12/25)
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  • Master's of Medical Product Development Management…

    San Jose State University (San Jose, CA)
    …following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs , clinical and medical affairs , quality ... career in clinical operations management, clinical trials monitoring, quality, regulatory , and the complex interdisciplinary process of medical product development.… more
    San Jose State University (05/06/25)
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  • Senior Director, Clinical Pharmacology

    Bristol Myers Squibb (San Diego, CA)
    …plan consistent with the development strategy, program goals, and the US/ international regulatory guidance for radiopharmaceuticals. + Collaborate with DMPK, ... team and closely collaborate with Clinical Operations, Clinical Development, Biometrics, and Regulatory Affairs . + Contribute to the design and execution of… more
    Bristol Myers Squibb (05/25/25)
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