Lead Quality Document Control & Compliance
Listed on 2026-09-20
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Biovire, Inc. in Brighton, Michigan seeks a Quality Document Control Supervisor to lead the QDC function for pharmaceutical drug product and medical device manufacturing.
Reporting to the Senior Manager, Quality Systems, you will manage master batch records, SOPs, change controls, and audits, ensuring compliance with cGMP and 21 CFR. This hands-on leadership role requires strong organization and cross-functional collaboration.
We are looking to fill the Lead Quality Document Control & Compliance position at Biovire, Inc. in MI, United States.
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