- Medtronic (Lafayette, CO)
- …Have: Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry OR a ... to technical documents to support CE marking and other global product registrations as necessary + Interact and negotiate...Masters degree with 2+ years of regulatory affairs experience in the medical device , biotech… more
- Dentsply Sirona (Milford, DE)
- …Years and Type of Experience: + 5(+) years of experience in regulatory affairs , preferably in the medical device industry. + Experience with leading ... care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina, USA....+ Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited… more
- Bayer (Washington, DC)
- …technology and strategic regulatory leadership. As the Director of Regulatory Affairs , you will represent our medical device regulatory team within ... + Compliance & Policy Contribution: Actively contribute to shaping global regulatory compliance policies and procedures that...quality systems are required + Direct professional experience in Regulatory Affairs within the medical device… more
- Abbott (Sylmar, CA)
- …Opportunity** Our location in Sylmar, CA currently has an opportunity for a Senior Regulatory Affairs Specialist-China. As a Senior Regulatory Affairs ... You'll Work On * As the Senior Specialist in Regulatory Affairs Sub-Function, considered as highly experienced...regulatory compliance, R&D, and/or quality experience in medical device industry + Good working knowledge of the product… more
- West Pharmaceutical Services (Exton, PA)
- Senior Regulatory Affairs Specialist Requisition ID: 71673 Date: Nov 4, 2025 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... and planet through our sustainability efforts. **Job Summary** The Sr. Specialist, Regulatory Affairs , Medical is responsible for influencing department … more
- Abbott (Plymouth, MN)
- …with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist** to join our team on-site in Plymouth, ... Abbott is a global healthcare leader that helps people live more... affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces… more
- West Pharmaceutical Services (Exton, PA)
- Sr. Specialist, Regulatory Affairs , Product Stewardship Requisition ID: 69466 Date: Nov 8, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... through our sustainability efforts. **Job Summary** The Sr. Specialist, Regulatory Affairs evaluates supplier regulatory ...(eg California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for all West global product… more
- J&J Family of Companies (Santa Clara, CA)
- …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... Description:** Johnson & Johnson is hiring for a **Principal Regulatory Affairs Specialist- Shockwave Medical** to join...demonstrate compliance. + Advises management on trends in the global regulatory environment that may impact current… more
- Abbott (Alameda, CA)
- …for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Regulatory Affairs Manager - APAC** position will work on-site at ... their glucose levels with our new sensing technology. This ** Regulatory Affairs Manager - APAC** position will...Care product portfolio in the APAC region, creating robust global regulatory strategies, working with cross-functional teams… more
- Danaher Corporation (Richmond, IL)
- …System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Regulatory Affairs Specialist for Leica Biosystems ... (QMS) to ensure ongoing compliance while continuing to develop regulatory affairs skills. This position reports to...experience. + Minimum of two years' experience within medical device /IVD, across a variety of regulatory submissions,… more