• Quality Assurance Manager

    Abbott (Temecula, CA)
    …+ 3-5 years in a supervisory/leadership role. + Class III or II medical device experience. + Demonstrated performance and results nonconformance management and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (12/10/25)
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  • Associate Clinical Research Specialist

    Kelly Services (Irvine, CA)
    …or equivalent is desired. + Clinical/ medical background is a plus. + Medical device experience is a plus. **Functional and Technical Competencies** **:** + ... a Kelly FSP employee you may be eligible for Medical , Dental, Vision, 401K and a variety of other...to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones + Supports the… more
    Kelly Services (12/03/25)
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  • Regulatory Affairs Surveillance Specialist

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …regulatory surveillance related to licensing activities, Source Plasma collection and medical device regulations. + Maintain up-to-date knowledge of regulatory ... and other regulatory submissions to ensure that Grifols Plasma Operations is in compliance with organizations similar to or including the US Food and Drug… more
    Grifols Shared Services North America, Inc (10/03/25)
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  • Regional Sales Manager - Abbott Diabetes Care

    Abbott (Los Angeles, CA)
    …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... improve people's health. We're always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do… more
    Abbott (12/10/25)
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  • Senior Clinical Scientist (GIS)

    Olympus Corporation of the Americas (Westborough, MA)
    …degree in life sciences or related field. + Minimum of 8 years medical device industry experience post-degree preferably in Clinical Affairs/Operations, ... ​ Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill… more
    Olympus Corporation of the Americas (12/04/25)
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  • Regional Sales Manager-Interventional /Peripheral…

    Teleflex (Baltimore, MD)
    …Attend regional and national medical meetings. * Adhere to and ensure the compliance of the Company's Code of Ethics, all Company policies which include but are ... :13101 **Interventional -** The Interventional business unit at Teleflex offers innovative medical devices that are used to diagnose and treat coronary and… more
    Teleflex (12/06/25)
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  • Principal, Regulatory Affairs - Transfusions

    Kelly Services (Norcross, GA)
    …within the past 8 years. * Knowledge of FDA 21 CFR 820, Health Canada Medical Device Regulations, MDSAP, and exposure to EU MDR/IVDR. * Strong writing, verbal ... for a Principal, Regulatory Affairs (Transfusion).** Principal, Regulatory Affairs - IVD / Medical Devices Location: Norcross, GA Industry: Medical Devices / In… more
    Kelly Services (11/08/25)
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  • Sterilization Control Assurer (12 Months fixed…

    Stryker (Arroyo, PR)
    …preferred). + Thorough understanding of QSR, ISO 13485, and other applicable medical device regulations, plus sterilization controls related standards (eg ISO ... cycles maintenance, sterilization cycle evaluation, product adoption and ensuring compliance to the applicable methods and regulatory standard requirements. **What… more
    Stryker (12/24/25)
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  • Director, Global Environmental, Product…

    Edwards Lifesciences (Irvine, CA)
    …regulations, product stewardship, or related field + Relevant industry experience (eg, medical device , pharmaceuticals, etc.) or in highly regulated environments ... will play a crucial role in supporting our environmental policies and ensuring compliance with relevant laws and regulations. You will also be responsible for… more
    Edwards Lifesciences (12/18/25)
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  • Director US Regulatory Global Strategic Labelling

    Lundbeck (Deerfield, IL)
    …+ Accredited Bachelor's Degree. + 10+ years of experience within a pharmaceutical, medical device and/or biotech industry, with 7+ years of experience in ... Chair for the Lundbeck Product Labelling Committee (LPLC) and related labelling compliance activities and may serve as liaison for cross functional governance… more
    Lundbeck (12/04/25)
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