Senior Regulatory Affairs – Medical Devices (Class III)

A leading medical device company is seeking a Senior/Principal Regulatory Affairs Specialist in Boston. This role involves developing regulatory strategies for pivotal trials and preparing submissions for FDA and EU approvals. The ideal candidate will have 5-7 years of regulatory experience in medical devices, particularly with FDA Class II and III submissions. Strong technical communication skills and a background in science or engineering are required. Competitive compensation aligned with experience will be offered. #J-18808-Ljbffr