Regulatory Affairs Specialist (NMPA)

This role serves as the Regulatory Affairs (RA) project lead for China, ensuring product registration compliance with NMPA standards and local regulations throughout the product lifecycle. The position involves coordinating cross-functional teams, managing pre- and post-market regulatory submissions, and maintaining critical documentation and trackers for medical device approvals. Key duties include developing regulatory strategies, communicating with stakeholders, and supporting internal audits and localization projects.