Regulatory Affairs Specialist - UDI Labeling - 239365
Medixâ„¢ - des moines, IA
Apply NowJob Description
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 internalexternal 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 UDIGUDID requirements.Qualifications:1+ years of UDI experience in medical devices.Experience with ERP systems (SAPOracle).Bachelors degree in life science or related field.Strong attention to detail, communication, and organizational skills.Join a growing team in the medical device industry today!
Created: 2025-02-21