Medical Device Regulatory Lead – FDA & Global Compliance

A leading recruitment platform is seeking a Principal Regulatory Affairs Specialist in New York City. This role involves developing regulatory strategies, ensuring product compliance, and leading submissions, particularly for medical devices. Candidates should have over 7 years of experience in regulatory affairs and medical device submissions, along with strong communication skills and project management abilities. The position offers competitive salary and an attractive benefits package, along with opportunities for professional growth. #J-18808-Ljbffr