• Global Supplier Quality Engineer…

    Danaher Corporation (Brea, CA)
    …risks. + Collaborate with cross-functional teams across R&D, Procurement, Operations, Quality, and Regulatory Affairs to embed quality into all phases of the ... meet quality, delivery and cost objectives . This position reports to the Sr. Director of Global Supplier Quality responsible for glob al supplier quality… more
    Danaher Corporation (08/19/25)
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  • Head of Quality & Compliance, Monarch Platform

    J&J Family of Companies (Santa Clara, CA)
    …teams including but not limited to R&D, Supply Chain/Manufacturing, Clinical and Medical Affairs , Regulatory Affairs , Service, Marketing, in furthering new ... our Monarch platform. This role will directly report to Global VP of Q&C Robotics and Digital Surgery and...but not limited to R&D, Operations, Commercial, Supply Chain, Regulatory Affairs , Medtech/Enterprise, to assure quality and… more
    J&J Family of Companies (08/08/25)
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  • Sr. Manager, Professional Education - JJMT…

    J&J Family of Companies (Irvine, CA)
    …and specialists, collaborating with multiple cross-functional partners including Marketing, Medical Affairs , Clinical Teams, Regulatory Affairs , and Sales ... use of J&J Neurovascular products. Reporting directly to the Director of Education, you will oversee a dynamic team...Embolic System and Enterprise Vascular Reconstruction Device with Clinical Affairs , Regulatory , and Legal teams. + Oversee… more
    J&J Family of Companies (08/26/25)
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  • T1D Immunology Medical Science Liaison, San Diego,…

    Sanofi Group (San Diego, CA)
    …portfolio and enhance patient outcomes. Reporting to the T1D Immunology Field Medical Director , this role will be responsible for the creation of impactful account ... solutions to meet those needs. We are an innovative global healthcare company with a focus on immunology that...scientific mindset. + Collaborate closely with the Field Medical Director to co-create robust, impactful plans for the key… more
    Sanofi Group (08/15/25)
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  • Senior Clinical Research Scientist

    Danaher Corporation (Sunnyvale, CA)
    …member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is ... possible. The Senior Clinical Research Scientist reporting to the Director , Clinical Research, develops and independently writes clinical documentation including… more
    Danaher Corporation (06/11/25)
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  • Senior Manager, Government Relations

    Lightsource bp (San Francisco, CA)
    …of government affairs . The position reports to, and works closely with, the director of government affairs in the US to help develop and execute state ... - and we're on a mission to become a global leader in onshore renewables, anchored by our proven...our growing US portfolio. The senior manager of government affairs role requires coordination with both internal and external… more
    Lightsource bp (08/23/25)
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  • Program Lead II, Clinical Program Development

    AbbVie (Irvine, CA)
    …cross-functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs/SDs. + Key contributor to ... Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and operations to bring… more
    AbbVie (07/11/25)
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  • Sr. Manager, Office of Ethics and Compliance

    Abbott (Sylmar, CA)
    …8-10 years of experience with exposure to business functions such as compliance, legal, regulatory affairs , governmental affairs , and/or finance. + Must have ... Abbott is a global healthcare leader that helps people live more...the following with minimal supervision from the OEC Senior Director : + Partners with all levels of key divisional… more
    Abbott (08/22/25)
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  • Program Safety Lead, GPS Medical Science - Job ID:

    Ascendis Pharma (Palo Alto, CA)
    …knowledge of FDA, EMA PV regulations, ICH Guidelines, and other applicable regulatory guidance documents; working knowledge of global safety regulations. + ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...laws and regulations and as appropriate, local and foreign regulatory reporting requirements and for signal detection, evaluation and… more
    Ascendis Pharma (07/17/25)
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  • ICSR Management Lead-Contractor - Job ID: Icsrc

    Ascendis Pharma (Palo Alto, CA)
    …validated Drug Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Working knowledge of FDA ... safety regulations, ICH Guidelines, and other applicable regulatory guidance documents; working knowledge of global safety regulations. + Potentially may require… more
    Ascendis Pharma (08/09/25)
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