Regulatory Affairs Manager

What you’d do

Manage regulatory affairs for medical device new product development projects, ensuring compliance with relevant regulations. This is a full-time role based in North Haven, Connecticut. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Bachelor's degree
• 5+ years medical device regulatory affairs experience
• Regulatory Affairs lead experience for new product development
• Engineering degree or advanced degree
• Full-time schedule