Senior Regulatory Affairs Specialist

What you’d do

Prepares and manages regulatory submissions to market new or modified medical devices and in vitro diagnostics in US and international markets, and develops procedures so product development and clinical studies meet regulatory requirements. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Regulatory submissions for medical devices/IVDs
• Domestic and international market experience
• Clinical study regulatory requirements
• Procedure and systems development