Associate Regulatory UDI Operations

This role supports the operational implementation and maintenance of the Unique Device Identification (UDI) program, ensuring compliance with US FDA regulations and other applicable standards. The position involves collecting and verifying UDI data, collaborating with cross-functional teams, and assisting in the development of regulatory submissions and quality management system integrations. The incumbent will also help maintain procedures, provide training, and propose process improvements to enhance data accuracy and compliance.