Senior Regulatory Affairs Specialist – Global Submissions

A medical device leader seeks a Senior Regulatory Affairs Specialist in Montvale, NJ. This role involves ensuring compliance with global regulatory standards for endoscopic products, collaborating across teams, and managing FDA submissions. Candidates should have 3-5 years of regulatory experience, a relevant degree, and exceptional communication skills. The company offers a collaborative work environment and a comprehensive benefits program, promoting growth and support for its team. #J-18808-Ljbffr