• Regulatory Affairs Specialist

    Kelly Services (Irvine, CA)
    ** Regulatory Affairs Specialist II (hybrid)** The Regulatory Affairs Specialist III, will provide administrative and technical support to ... compliance with US and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory support… more
    Kelly Services (06/29/24)
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  • Senior Specialist , Regulatory

    Edwards Lifesciences (Irvine, CA)
    …maintaining regular, in-person collaboration. **How you'll make an impact:** As a Senior Specialist , Regulatory Affairs , you work with other functional areas ... patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative...understanding of domestic and global regulations relevant to Class II and/or Class III medical devices Aligning our overall… more
    Edwards Lifesciences (07/10/24)
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  • Specialist , Regulatory

    Edwards Lifesciences (Irvine, CA)
    …and be part of our inspiring journey. **How you will make an impact:** As a Specialist , Regulatory Affairs for TMTT, you will complete and maintain clinical ... patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative...understanding of global regulations relevant to medical devices, Class II and/or Class III + Solid knowledge of global… more
    Edwards Lifesciences (06/04/24)
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  • Regulatory Affairs Specialist

    Actalent (Laguna Hills, CA)
    Description: This position is a regulatory affairs specialist for a medical device company. Individual must be knowledgeable in medical device industry and ... have Class II or Class III device experience. Candidate will: Prepare...maintain Adagio compliance. Post-market and vigilance reporting process. Represent Regulatory Affairs on Engineering & R&D product… more
    Actalent (07/10/24)
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  • Senior Specialist , Regulatory

    Edwards Lifesciences (Irvine, CA)
    …at Edwards' Irvine campus. **How you will make an impact:** * Represent the regulatory function on manufacturing and product development teams to provide input on ... regulatory requirements, including presenting alternatives for meeting ...EU and US regulations relevant to medical devices, Class II and/or Class III devices * Full knowledge and… more
    Edwards Lifesciences (06/30/24)
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