• Quality Systems Documentation Specialist

    Terumo Medical Corporation (Elkton, MD)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Quality Systems Documentation Specialist Date: Aug 28, 2025 Req ID: 5117...Familiarity with audit processes and regulatory requirements within the medical device industry. + Proficiency in document… more
    Terumo Medical Corporation (08/28/25)
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  • Principal CoreValve Therapy Development…

    Medtronic (Orlando, FL)
    …with experience coordinating programs + Thorough working knowledge of medical terminology, medical procedures and the medical device industry + Excellent ... CHANGE** **LIVES -** **POSITION DESCRIPTION:** The CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical , educational and sales… more
    Medtronic (09/11/25)
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  • SAP Extended Warehouse Mgmt Specialist

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... SAP Extended Warehouse Mgmt Specialist Date: Sep 2, 2025 Req ID: 4412...Removal Strategies, Post Processing Framework, Replenishment, Physical Inventory. + Medical Device /Serialized product experience is required +… more
    Terumo Medical Corporation (08/13/25)
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  • Senior Field Intervention Specialist

    Teleflex (Morrisville, NC)
    clinical research. * Additional experience in clinical setting, biostatistics, IDE clinical studies or medical device product support. * Demonstrate ... Senior Field Intervention Specialist (REMOTE) **Date:** Sep 9, 2025 **Location:** Morrisville,...both peripheral vascular and coronary products, including product-specific and clinical protocol training, data collection and study device more
    Teleflex (09/10/25)
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  • Regulatory Specialist

    Globus Medical, Inc. (Audubon, PA)
    …is a plus + Minimum of 2-5 years' experience in Regulatory Affairs in the medical device industry, , preferably within orthopedic medical devices; + ... At Globus Medical , we move with a sense of urgency...response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the… more
    Globus Medical, Inc. (06/25/25)
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  • CDO Specialist #1

    ManpowerGroup (Indianapolis, IN)
    …Description Summary The Connected Device Onboarding Specialist II provides clinical evaluation services to further medical device security efforts of ... TRIMEDX clients. The Connected Device Onboarding Specialist II is routinely expected to conduct hands-on examination...Office and service management software Skill in determining how medical device security features should function and… more
    ManpowerGroup (09/05/25)
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  • Senior Grants and Contracts Specialist

    Mount Sinai Health System (New York, NY)
    …distribution of funding opportunities packets, calendars and special alerts. + Contracts Specialist Negotiate clinical trial agreements and amendments on behalf ... the integration of the latest discoveries in the lab and innovations in clinical care into patient-centric care models in the safest, and most compassionate way… more
    Mount Sinai Health System (08/20/25)
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  • Healthcare Compliance Contract Specialist

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Healthcare Compliance Contract Specialist Date: Aug 21, 2025 Req ID: 4968...management system is a plus + Experience specifically in medical device contracting environment strongly preferred +… more
    Terumo Medical Corporation (07/24/25)
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  • Biomedical Equipment Support Specialist

    Veterans Affairs, Veterans Health Administration (Orlando, FL)
    …the facility's medical device protection program. Ensures networked medical equipment and clinical systems are inventoried in the appropriate database. ... Summary The selected Biomedical Equipment Support Specialist (BESS) will specialize in information systems within...include, but are not limited to; Manages projects involving medical equipment and clinical systems, to include… more
    Veterans Affairs, Veterans Health Administration (09/13/25)
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  • Senior Regulatory Affairs Specialist

    Abbott (Plymouth, MN)
    …help of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly with ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (08/18/25)
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