Medical Device Regulatory Lead – FDA & Global Compliance

A partner company seeks a Principal Regulatory Affairs Specialist to lead the development of regulatory strategies affecting product introduction and compliance. This role requires extensive knowledge of U.S. and international standards, as well as medical device regulations. The ideal candidate will have over 7 years in regulatory affairs, experience with FDA submissions, and strong communication skills. The position offers competitive salary and comprehensive benefits, emphasizing the importance of regulatory compliance in product development. #J-18808-Ljbffr