Lead Regulatory Strategist, Catheter Medtech (Hybrid OC)

A medical device firm is looking for a Principal Regulatory Affairs Specialist to lead global regulatory strategy for Class III catheter-based devices. This high-impact role requires a candidate with 8–12+ years of experience in Regulatory Affairs, particularly with PMA and IDE submissions. The position is hybrid, based in Orange County, CA, and offers a unique opportunity to shape regulatory strategy from development to market entry, making a direct impact on approvals and commercialization. #J-18808-Ljbffr