Regulatory Affairs Leader - Medical Devices, 510(k)/PMA Expert

A partner company located in New York seeks a Principal Regulatory Affairs Specialist to develop and implement regulatory strategies for new and existing products. This role involves maintaining compliance with U.S. and international standards, leading regulatory submissions, and guiding the regulatory team. Candidates should have 7+ years of experience in regulatory affairs, particularly with medical devices, and strong communication skills. Competitive salary and comprehensive benefits are offered. #J-18808-Ljbffr