Quality Document Control Lead - GMP & Audit Readiness
Listed on 2026-10-06
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Quality Engineering
Biovire is seeking a Quality Document Control Supervisor to lead the controlled documentation program for pharmaceutical drug product and medical device manufacturing at our Brighton, Michigan site. This hands-on role oversees Master Batch Records, SOPs, and archival processes in a fast-paced GMP environment.
The successful candidate will drive document control improvements, support audits, and collaborate across Quality, Manufacturing, and Process Engineering to ensure accurate, controlled
We are looking to fill the Quality Document Control Lead - GMP & Audit Readiness position at Bryllan LLC in Brighton, MI, United States.
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This posting is for the Quality Document Control Lead - GMP & Audit Readiness role at Bryllan LLC, based in Brighton, MI, United States.
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