Global Regulatory Affairs Associate, Medical Devices (FDA)

A leading regulatory compliance firm in New York is seeking a Regulatory Affairs Specialist to manage regulatory submissions and maintain compliance with FDA standards. The ideal candidate will have at least 4 years of experience in Regulatory Affairs within the medical device sector. Responsibilities include conducting assessments for product changes, managing registrations, and collaborating with stakeholders to ensure timely submissions. The role requires excellent communication skills and fluency in English. #J-18808-Ljbffr