Regulatory Affairs Specialist, Medical Devices (Hybrid)

A medical device company located in New York is seeking a Staff Regulatory Affairs Specialist to manage regulatory strategies for product approvals. The ideal candidate has at least 5 years of regulatory experience in the medical device industry and a university degree. Responsibilities include authoring regulatory submissions, advising on regulatory strategies, and ensuring compliance. This position offers a competitive salary and a hybrid work model, with responsibilities for relocating being the candidate's own. #J-18808-Ljbffr