What are the responsibilities and job description for the Regulatory Affairs Specialist - UDI Labeling - 239365 position at Medix?
Regulatory UDI Operations Specialist
We are seeking a Regulatory UDI Operations Specialist to support UDI program implementation and compliance with FDA and global regulations in the medical device industry. This role collaborates with Regulatory Affairs, Supply Chain, R&D, QA, and Marketing to ensure accurate UDI data management.
Key Responsibilities :
- Collect, verify, and enter UDI data into internal / external databases.
- Ensure data accuracy between labels and master UDI data.
- Assist in implementing UDI-compliant solutions and updating SOPs.
- Support process improvements for regulatory data accuracy.
- Provide training on UDI / GUDID requirements.
Qualifications :
Join a growing team in the medical device industry today!
