Global Medical Device Regulatory Specialist

A medical device company based in Bedford, MA is seeking a Regulatory Specialist to support the development and compliance of medical devices. The role entails preparing and submitting regulatory filings, maintaining device listings, and collaborating with product development teams to ensure regulatory requirements are integrated. Ideal candidates will possess a BA or BS in a scientific field and have 1-2 years of regulatory experience in the medical device sector. Strong communication and technical writing skills are essential. #J-18808-Ljbffr