• Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    …innovation in a more connected, compassionate world. **A Day in the Life** The Sr Regulatory Affairs Specialist will play a key role in sustaining the current ... that our product technical documentation is current and accurate. **SENIOR REGULATORY AFFAIRS SPECIALIST - NEUROVASCULAR** In the Neurovascular Operating… more
    Medtronic (07/29/25)
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  • SCI Senior Regulatory Specialist

    Stanford University (Stanford, CA)
    SCI Senior Regulatory Specialist (Hybrid) **School of Medicine, Stanford, California, United States** **New** Administration Post Date 3 days ago Requisition # ... 106985 **Senior Regulatory Specialist - Cancer Cell Therapy (Hybrid)**...teamwork, and superb attention to detail. We strive for top- quality regulatory support of investigator-initiated clinical trials… more
    Stanford University (08/07/25)
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  • Principal Regulatory Affairs…

    J&J Family of Companies (Santa Clara, CA)
    …States of America **Job Description:** Johnson & Johnson is hiring for a **Senior Regulatory Affairs Specialist (Remote) - Shockwave** to join our team. This is ... of sonic pressure waves for the treatment of calcified plaque. The Principal Regulatory Affairs Specialist is an individual contributor that works closely and… more
    J&J Family of Companies (08/08/25)
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  • Senior Regulatory Affairs Specialist

    Abbott (Santa Clara, CA)
    …catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite opportunity working out ... the Abbott Vascular Division. As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory more
    Abbott (07/29/25)
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  • Clinical Research Regulatory

    University of Southern California (Los Angeles, CA)
    Regulatory SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Clinical-Research- Regulatory - ... study and clinical research documentation to support principal investigators and quality assurance systems for the Clinical Investigations Support Office. Provides … more
    University of Southern California (07/11/25)
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  • Sr. Specialist , Regulatory Affairs

    Terumo Neuro (Aliso Viejo, CA)
    **12814BR** **Title:** Sr. Specialist , Regulatory Affairs **Job Description:** Responsible for preparing strategy for worldwide product approval submission ... 6. Ability to comprehend technical documents and concepts. **External-Facing Title:** Sr Specialist , Regulatory Affairs **Posting Country:** US - United States… more
    Terumo Neuro (08/09/25)
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  • Medical Devices, Regulatory

    Meta (Burlingame, CA)
    …wrist wearables, and other innovative devices. **Required Skills:** Medical Devices, Regulatory Specialist Responsibilities: 1. Interact directly with FDA and/or ... **Summary:** We're seeking a regulatory affairs specialist to join our...Directive/EU MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards 10. Advanced… more
    Meta (08/01/25)
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  • Principal Regulatory Affairs…

    Medtronic (Santa Rosa, CA)
    …and influences the preparation of documentation to support innovative and high- quality regulatory submissions from early phase strategies, marketing ... role will be based in Santa Rosa, CA. The **Principal Regulatory Affairs Specialist ** will support Research and Development programs with early phase pre-market… more
    Medtronic (07/25/25)
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  • Principal Regulatory Affairs…

    Medtronic (Los Angeles, CA)
    …questions from regulatory agencies. As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory ... regulatory requirements as they relate to the product portfolio and regulatory and quality system procedures. + Prepare regulatory submissions for new… more
    Medtronic (08/08/25)
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  • Regulatory Affairs Specialist

    Envista Holdings Corporation (Brea, CA)
    **Job Description:** The ** Regulatory Affairs Specialist ** is responsible for assembling CE Technical files and final review of deliverables for MDR ... Works in partnership with manufacturing and RA/QA in designing and enhancing quality management systems to facilitate overall regulatory compliance. +… more
    Envista Holdings Corporation (06/03/25)
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