• Medical Device Regulatory…

    Abbott (Santa Clara, CA)
    …executives, and scientists. **The Opportunity** We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (09/06/25)
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  • Manager, Regulatory Affairs…

    J&J Family of Companies (Santa Clara, CA)
    …to efficiently and effectively meet assigned regulatory requirements for Shockwave Medical Inc. (SWMI). The Regulatory Affairs Manager combines knowledge ... health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** ...aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease… more
    J&J Family of Companies (09/03/25)
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  • Senior Regulatory Affairs Specialist…

    Stryker (Redmond, WA)
    …in Regulatory Affairs ) + Previous experience with Class II/III medical devices + Experience authoring regulatory submissions for product approval ... Washington.** **What you will do** As part of the Medical Regulatory Affairs team, you...team, you will work with the team to maintain medical devices on the market and ensure… more
    Stryker (09/08/25)
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  • Regulatory Affairs Specialist,…

    Hologic (Louisville, CO)
    Regulatory Affairs Specialist, Medical Device Louisville, CO, United States Marlborough, MA, United States **Join Hologic's Surgical Division as a ... industry. **What You'll Bring:** **Experience** + 2-5 years in regulatory affairs , preferably within the medical device industry. + Proven experience… more
    Hologic (09/05/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    …Medical Device Experience:** Minimum of 4 years of relevant experience in medical device regulatory affairs . + **510(k) Submission Experience:** ... or university required; advanced degree with a minimum of 2 years of experience in medical device regulatory affairs is a plus. + ** Regulatory … more
    Medtronic (09/09/25)
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  • Regulatory Affairs Associate II

    Terumo Aortic (Sunrise, FL)
    …(or related field) from an accredited college or university and 3 years direct experience in medical device regulatory affairs + Minimum 5 years direct ... experience in medical device regulatory affairs if no...and Design Dossiers/Technical files) for Class II and III medical devices and a successful track record… more
    Terumo Aortic (08/22/25)
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  • Sr. Lead Specialist, Regulatory…

    GE HealthCare (Madison, WI)
    …by the Regulatory Affairs Professionals Society (RAPS). + Experience in medical device regulatory affairs + Demonstrated life-long learner; ... pulse oximetry. You will work within a team of Regulatory Affairs professionals to ensure GE HealthCare...labeling compliance, etc. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is… more
    GE HealthCare (07/10/25)
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  • Principal Regulatory Affairs…

    Abbott (St. Paul, MN)
    …**Qualifications** + Minimum of 5 years' experience working with Class II and/or Class III medical devices . Regulatory Affairs Certification (RAC) is a ... and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist** to join Abbott's Vascular... regulatory submissions for Pharmaceutical, In vitro diagnostic devices and/or medical devices . +… more
    Abbott (08/23/25)
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  • Senior Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    …**You're the right fit if:** + You've acquired 5+ years of experience in the medical device regulatory affairs and/or quality assurance field. Experience ... **Senior Regulatory Affairs Specialist (Ultrasound)** The Senior Regulatory Affairs Specialist recommends process improvements, updates regulatory … more
    Philips (08/29/25)
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  • Regulatory Affairs Specialist

    Astrix Technology (Fort Worth, TX)
    …EC Certificates (MDD /MDR) and associated documentation. **Key Requirements:** + 4+ years in medical device regulatory affairs + Experience with European ... ** Regulatory Affairs Specialist** Clinical Fort Worth,...compliance and lifecycle change management for medical devices . + Works closely with site regulatory … more
    Astrix Technology (08/11/25)
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