Global Regulatory Affairs Lead — Medical Devices

A leading medical device company in Covington, Georgia, seeks a Senior Regulatory Affairs Specialist. This role involves developing and executing regulatory strategies for medical devices, including preparing submissions to the FDA and European regulatory bodies. The candidate should possess a Bachelor's in a relevant field and have a minimum of 5 years of experience in regulatory affairs, especially in medical devices. Strong technical writing, project management skills, and knowledge of U.S. and European regulations are essential. #J-18808-Ljbffr