Hybrid Regulatory Affairs Specialist - Medical Devices

A leading medical devices company is seeking a Regulatory Affairs Specialist to join their team based in Irvine, CA. The candidate will be responsible for planning and implementing regulatory submissions while ensuring compliance with healthcare regulations. They will also interact with regulatory bodies to facilitate product approvals and contribute to the strategic regulatory pathway development. Ideal applicants should possess expertise in regulatory affairs and work independently with minimal supervision. #J-18808-Ljbffr