Senior Medical Device Regulatory Lead - 510(k)/PMA Expert

A leading healthcare consultancy is seeking a Principal Regulatory Affairs Specialist in New York. This role involves developing regulatory strategies for product introductions and ensuring compliance with U.S. and international standards. Responsibilities include leading submission activities for device clearances, interpreting regulatory requirements, and managing compliance with existing products. Ideal candidates will have a Bachelor’s Degree along with 7+ years of experience in regulatory affairs and medical device knowledge. A competitive salary and flexible benefits are provided. #J-18808-Ljbffr