Quality Systems & Document Control Lead
ADP, Inc.
ProMed is seeking a Quality Systems Specialist to manage the day-to-day document control within the Quality Management System, ensuring ISO 13485 and FDA 21 CFR 820/Part 11 compliance. You will drive continuous improvements in the QMS to support manufacturing operations and audit readiness. The role involves overseeing change management, training coordination, and ensuring controlled documents are current, approved, and properly archived in a regulated environment. #J-18808-Ljbffr ADP, Inc.
Vacancy posted 5 days ago
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