The Regulatory Affairs Specialist II

What you’d do

Regulatory affairs role supporting medical device submissions and compliance with US FDA and European medical device regulations. Full time, based in West Chester, Pennsylvania. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• BA/BS degree
• 2+ years regulatory affairs experience in medical devices
• US FDA regulations experience
• European Medical Device Regulations experience