• Product Marketing Internship

    Nissha Medical Technologies (Buffalo, NY)
    …research and competitive analysis to support marketing plans for domestic and international medical products. 3. Collaborate with product marketing, corporate ... internship offers hands-on experience in marketing and product management for medical products, focusing on customer segmentation, market research, and campaign… more
    Nissha Medical Technologies (11/14/25)
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  • Registered Nurse - International Clinical…

    Cedars-Sinai (Los Angeles, CA)
    … Clinical Program Coordinator - 8 Hour Days **Department** : Cedars Sinai International **Business Entity** : Cedars-Sinai Medical Center **Job Category** : ... 19 years in a row for providing the highest-quality medical care in Los Angeles. We also were awarded...What you will be doing in this role: The International Clinical Coordinator provides vital education and information on… more
    Cedars-Sinai (10/30/25)
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  • Regulatory Affairs Specialist II

    Abbott (Pleasanton, CA)
    …detail. + Maintains ongoing surveillance and analysis of all pertinent international medical device regulations to ensure submission requirements world-wide ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (10/09/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …+ Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide ... and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Experience with risk management, design… more
    Abbott (09/27/25)
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  • Senior Payroll & Benefits Specialist

    St. George's University (Denver, CO)
    …(USS) is an affiliate of St. George's University (SGU), a leading provider of international medical education. SGU students and faculty come from 151 countries ... Payroll and Benefits supports comprehensive payroll processing for both US and international employees and assists in the administration of the benefits program. The… more
    St. George's University (11/15/25)
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  • Director of Admissions, US

    St. George's University (Great River, NY)
    …(USS) is an affiliate of St. George's University (SGU), a leading provider of international medical education. SGU students and faculty come from 151 countries ... admissions strategies that may be tailored by region (US, Canada, or International ) to meet market opportunities, program demands, and enrollment goals. This… more
    St. George's University (10/10/25)
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  • Senior Regulatory Affairs Specialist - Heart…

    Abbott (Pleasanton, CA)
    …applications, PMA supplements and US device regulations, or with EU and other international medical device regulations and submissions. + Must be familiar with ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (10/11/25)
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  • Regulatory Affairs Specialist II…

    Abbott (Plymouth, MN)
    …to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (11/22/25)
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  • Regulatory Affairs Manager - Heart Failure…

    Abbott (Pleasanton, CA)
    …or PMA supplements and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Ability to work in a ... working knowledge of regulatory requirements for US, EU (EU MDR), and other international geographies. + Experience with medical device software requirements and… more
    Abbott (11/15/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Lafayette, CO)
    …Design Dossier and/or Technical Documentation experience + Technical Writing + International medical device regulatory submission/approval experience, to include ... regulatory change assessments, and supporting the implementation of the EU Medical Device Regulation (MDR). The Sr. RAS translates regulatory requirements into… more
    Medtronic (11/18/25)
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