Senior Regulatory Affairs Lead - Medical Devices (Hybrid)

A leading medical device company in New York seeks a Senior Staff Regulatory Affairs Specialist. The candidate will guide regulatory strategy and ensure compliance throughout the product lifecycle. Responsibilities include preparing regulatory submissions, collaborating with cross-functional teams, and leading negotiations with regulatory authorities. The ideal candidate should have at least 7 years of experience in regulatory roles within the medical device industry and possess a university degree and RAC certification. This position offers a hybrid work model.#J-18808-Ljbffr