Senior Medical Device Regulatory Lead

A leading staffing agency is seeking a Principal Regulatory Affairs Specialist to support regulatory strategies for product development and compliance. The successful candidate will have at least 7 years of experience in regulatory affairs and medical device experience. Key responsibilities include guiding regulatory staff, ensuring compliance with U.S. and international standards, and leading 510(k) or PMA submissions. This position offers competitive compensation and benefits in a supportive work environment. #J-18808-Ljbffr