Senior Regulatory Affairs Specialist

What you’d do

Support regulatory affairs for medical devices, working with U.S. FDA and EU MDR requirements and guidance. Full time role based in West Chester, PA, with other listed U.S. locations. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 2+ years regulatory affairs or medical device experience
• 2+ years medical device industry experience
• Familiarity with U.S. FDA regulations
• Knowledge of EU MDR/MDD