Global Regulatory Affairs Lead – Medical Devices & IVD

A medical technology firm in California is seeking a Regulatory Affairs Specialist to manage international product registrations and ensure compliance across markets. The ideal candidate will have over 5 years of experience in regulatory affairs, specifically in medical devices or pharma, strong project management skills, and a solid understanding of global regulatory frameworks. This role also includes preparing registration dossiers and supporting audits, making a meaningful impact in bringing innovative products to the market. #J-18808-Ljbffr