• Medical Device Regulatory

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

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …in translational medicine (T0 - T1) or early development (phase 1) assets either within Medical Affairs , Regulatory Affairs , or Clinical Development is ... Medical Director of CNS Early Assets, Global Medical Affairs , responsible for certain assets within...evidence, US and global commercial teams, market access, and regulatory affairs , to ensure integrated global strategies… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Head Pharmacovigilance & Medical

    Dr. Reddy's Laboratories (Princeton, NJ)
    …industry **Skills & attributes:** + Understanding of North American pre-and post-marketing regulatory requirements for medical Affairs and Medical ... Drug Discovery and Development Processes; Clinical Development Tools and Processes; Medical Affairs Guidelines; Regulatory Guidelines; Pharmacovigilance… more
    Dr. Reddy's Laboratories (08/19/25)
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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:** Proven ... required; advanced degree with a minimum of 2 years of experience in medical device regulatory affairs is a plus. + ** Regulatory Knowledge:** Excellent… more
    Medtronic (09/09/25)
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  • Regulatory Affairs Associate II

    Terumo Aortic (Sunrise, FL)
    …field) from an accredited college or university and 3 years direct experience in medical device regulatory affairs + Minimum 5 years direct experience ... Regulatory Affairs Associate II Date: Aug 21, 2025...in medical device regulatory affairs if no degree. + Knowledge of US and European … more
    Terumo Aortic (08/22/25)
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  • Sr. Lead Specialist, Regulatory

    GE HealthCare (Madison, WI)
    Regulatory Affairs Certification (RAC) issued by the Regulatory Affairs Professionals Society (RAPS). + Experience in medical device regulatory ... 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)
    …+ Minimum of 5 years' experience working with Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus. + ... female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist** to join Abbott's Vascular Division on-site in… more
    Abbott (08/23/25)
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  • Senior Regulatory Affairs Specialist…

    Stryker (Redmond, WA)
    …Monday through Wednesday in **Redmond, Washington.** **What you will do** As part of the Medical Regulatory Affairs team, you will work with the team to ... We are currently seeking a **Senior Regulatory Affairs Specialist** to join our ** Medical ** **Division**...certification or Advanced Degree (Masters in Regulatory Affairs ) + Previous experience with Class II/III medical more
    Stryker (09/08/25)
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  • Senior Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    …the right fit if:** + You've acquired 5+ years of experience in the medical device regulatory affairs and/or quality assurance field. Experience authoring ... **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 MDR ... ** Regulatory Affairs Specialist** Clinical Fort Worth,...Supporting EU MDR compliance and lifecycle change management for medical devices. + Works closely with site regulatory more
    Astrix Technology (08/11/25)
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