- Medtronic (Santa Rosa, CA)
- …+ Bachelor's degree required with a + Minimum of 4 years of experience in medical device regulatory affairs experience + Or Advanced degree with 2 years of ... Mounds View, MN or Santa Rosa, CA. The **Senior** ** Regulatory Affairs Specialist** will support our innovative Transcatheter Tricuspid...heart valve products + Experience with Software as a Medical Device + RAC Medical Device Certification… more
- J&J Family of Companies (Irvine, CA)
- …Device Submissions and Assessment Experience **required** . + Experience with Vision related medical device regulatory _highly desired_ . + Working knowledge of ... be directed to your accommodation resource. \#LI-Hybrid **Required Skills:** Class III Medical Devices, Regulatory Approvals, Regulatory Processes, … more
- Teleflex (Morrisville, NC)
- …a science or engineering field, or equivalent work experience. * 5+ years of Medical Device Regulatory Affairs experience, domestic and international. 3 years of ... Senior Regulatory Affairs Specialist **Date:** Dec 2, 2025 **Location:**...:12987 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to… more
- Actalent (Lake Forest, CA)
- …US FDA, regulatory submission, Regulatory reporting, Test plan, Regulatory compliance, Compliance, Quality engineering, Medical device, Regulatory ... Description We are seeking an experienced and strategic Regulatory Affairs Manager to support global regulatory...development and sustaining activities. - Strong understanding of global medical device regulations (eg, FDA CFR, EU MDR). Skills… more
- ICON Clinical Research (NC)
- …development planning (PDP/RDP/CDP), scientific/agency advice, orphan drugs/pediatric development, medical devices, regulatory intelligence, due diligence, ... Senior Manager, Regulatory Affairs - IVD ICON plc is a...role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of Innovative… more
- West Pharmaceutical Services (Exton, PA)
- …Bachelor's with 5+ years required; or + Master's degree/PhD 2+ years medical device regulatory experience required **Preferred Knowledge, Skills and Abilities** ... Sr. Specialist, Regulatory Affairs, Product Stewardship Requisition ID: 69466 Date:...legislations (eg California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for all West global product portfolios… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …business units as needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing, ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …strategic legal advisor to multiple internal stakeholders, including the commercial, medical affairs, regulatory , HEOR, corporate affairs, and compliance teams. ... This position with the Regeneron Regulatory and Commercial Law team will provide proactive...client teams supported, and advising on strategic brand and medical planning, developing creative and innovative solutions to key… more
- Sanofi Group (Morristown, NJ)
- …or other relevant discipline + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs, with 5+ years specifically within advertising & ... cooperation without relying on authority, including participating in cross-functional groups ( medical , legal, regulatory , etc.) to lead toward decisions. +… more
- UTMB Health (Galveston, TX)
- …degree or equivalent and two years of experience in human/animal research, medical care, or regulatory affairs and effective written communication skills ... HRPP/IRB Office (Research, Regulatory , & Compliance - Galveston) **Galveston, Texas, United States** Business, Managerial & Finance UTMB Health Requisition # 2506691… more