• Medical Device Regulatory

    Oracle (Salt Lake City, UT)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (11/25/25)
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  • Regulatory Affairs Associate…

    GRAIL (Salt Lake City, UT)
    …management within the IVD, medical device , or pharmaceutical industries. + Regulatory affairs and IVD device experience preferred. + An advanced ... FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such...and international regulatory frameworks and processes for medical device development and approvals. + Effective… more
    GRAIL (12/03/25)
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  • Director, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …10+ years of progressively more responsible experience as a multi-functional Regulatory Affairs professional in the medical device industry + 10+ years' ... Become a **maker of possible** with us. The Director, Regulatory Affairs will be a member of... regulatory information + Comprehensive understanding of global medical device regulations, with in-depth knowledge of… more
    BD (Becton, Dickinson and Company) (11/16/25)
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  • Staff Specialist, Regulatory Affairs

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …**Minimum Requirements:** + Bachelor's degree or higher + 6-8 years' Regulatory Affairs experience in the medical device industry + Experience leading ... US, EU, and other global regulatory requirements are met + Evaluates medical device regulations and leads development of global regulatory strategies… more
    BD (Becton, Dickinson and Company) (10/23/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (Salt Lake City, UT)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Salt Lake City, UT)
    …+ Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device , cosmetics or ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
    Bausch + Lomb (09/06/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Salt Lake City, UT)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Postmarket Surveillance Manager

    BioFire Diagnostics, LLC. (Salt Lake City, UT)
    …broader quality goals and regulatory landscapes. + Deep understanding of global medical device /IVD regulations (eg, FDA 803/806, MEDDEV, QSR 820, ISO 13485) ... Fields) with 6 years of experience in a regulated medical device /IVD industry employment position such as...industry employment position such as post-market surveillance, quality assurance, regulatory affairs , clinical affairs or… more
    BioFire Diagnostics, LLC. (12/03/25)
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  • Human Factors Engineer - Remediation Focus

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …and develop **use-related risk analysis (URRA)** and mitigation strategies in partnership with Medical & Regulatory Affairs . + Collaborate with ** ... Validation &** **Human Factors strategies** for successful submission in concert with Regulatory Affairs . + Conduct **gap analyses** of existing DVal/HF… more
    BD (Becton, Dickinson and Company) (11/13/25)
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