Lead Quality Document Control & Compliance
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers
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.
Join us at Biovire, Inc. as our next Lead Quality Document Control & Compliance in MI, United States.
This is a genuine role to take on the Lead Quality Document Control & Compliance role at Biovire, Inc.
As a Lead Quality Document Control & Compliance, you will play an important part at Biovire, Inc. in MI, United States.
We invite applications for the Lead Quality Document Control & Compliance position located in MI, United States.
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