Reporting to the Senior Manager, Quality Systems, the Quality Document Control Supervisor will oversee and support regulated document control activities across Biovire, partnering closely with Quality, Manufacturing, Process Engineering, and other functions to ensure documentation is accurate, controlled, available, and maintained in accordance with cGMP and regulatory requirements. This is a hands-on Quality Systems leadership role with responsibility for controlled documentation, batch record issuance, document lifecycle management, archival and retention, and the day-to-day workflow of the Quality Document Control function.