Global Regulatory Affairs Lead, Medical Devices

A leading biotech company in Wilmington, North Carolina is seeking an experienced Regulatory Affairs professional. This role requires a Bachelor's degree and at least 5 years of experience in regulatory affairs or quality engineering in the medical device sector. Responsibilities include managing regulatory requests, conducting risk assessments, and supporting submissions. Ideal candidates will demonstrate strong technical writing skills and the ability to collaborate with cross-functional teams. A Regulatory Affairs Certification (RAC) is preferred. #J-18808-Ljbffr