Global Regulatory Affairs Specialist - Medical Devices

A global healthcare company in Morrisville is seeking a Regulatory Affairs Specialist to develop regulatory strategies and manage submissions for various products. The ideal candidate will have 2-3 years of regulatory affairs experience in a regulated environment, preferably with medical devices. Key responsibilities include ensuring compliance with regulatory requirements, interacting with authorities during the submission process, and managing product documentation. The role emphasizes strong analytical and communication skills, teamwork, and organizational abilities. #J-18808-Ljbffr