- Sanofi Group (Morristown, NJ)
- …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
- Takeda Pharmaceuticals (Lexington, MA)
- …councils, inspection support, and industry interactions. + Partner with critical stakeholders in Regulatory Affairs , Device Quality, and PharmSci to ensure ... medical devices, including stand-alone devices, combination devices, and Software as a Medical Device (SaMD). You will ensure that Quality System requirements… more
- West Pharmaceutical Services (Exton, PA)
- …+ Minimum of 8 years of experience in a scientific or regulatory affairs role within the pharmaceutical, biotechnology, or medical device industry. ... Manager, Scientific Affairs Requisition ID: 72136 Date: Dec 9, 2025...be involved in managing scientific projects, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to develop… more
- FleishmanHillard (Washington, DC)
- …intersection of healthcare and public affairs in service to pharmaceutical and medical device companies, as well as third party organizations to include ... Additional desired areas of expertise include issues advocacy and public affairs campaigns, strong writing skills, and stakeholder engagement with policy and… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …health science field or a different field with 4+ years of experience in the medical device clinical research industry. + 2+ years of experience managing and ... monitoring clinical research studies in the medical device industry. + Strong working knowledge of GCP, FDA regulations, and current industry practices related… more
- Veterans Affairs, Veterans Health Administration (Lexington, KY)
- …(COR) and maintain appropriate certification levels. Investigate, remediate and document Repairable Medical Device (RMD) recalls and safety alerts issued through ... Health Care System in Lexington, Kentucky. Works in support of the medical equipment management program. Troubleshoots and performs planned maintenance on medical… more
- Veterans Affairs, Veterans Health Administration (Indianapolis, IN)
- …including, but not limited to, node to server failures. Adheres to VA Medical Device Cyber Security policies and procedures in pre-procurement, during system ... as a purchase card holder, as required. Investigates, remediates and documents Repairable Medical Device (RMD) recalls and safety alerts issued through the VA… more
- Veterans Affairs, Veterans Health Administration (Beckley, WV)
- …conduct prepurchase evaluations and address pre-implementation security issues to ensure medical device isolation architecture (MDIA) requirements are met. They ... cases of equipment damage and abuse, equipment failure reports that cannot be duplicated, and medical device security incidents. They serve as a member of a Root… more
- Veterans Affairs, Veterans Health Administration (Syracuse, NY)
- …including, but not limited to, node to server failures. Adheres to VA Medical Device Cyber Security policies and procedures in pre-procurement, during system ... as a purchase card holder, as required. Investigates, remediates and documents Repairable Medical Device recalls and safety alerts issued through the VA Alerts… more
- Veterans Affairs, Veterans Health Administration (Hot Springs, SD)
- …all matters of concern relating to the facility wide lifecycle management of medical equipment. Responsibilities Major duties include, but are not limited to, the ... following: Manages the lifecycle of medical equipment and clinical systems. Functions include: technology assessment including defining requirements and analyzing… more
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