Quality Document Control Supervisor

Job overview

The Quality Document Control Supervisor role is onsite in Brighton, MI. Compensation is not specified. Biovire is advancing toward commercialization and is building quality systems to support pharmaceutical drug product and medical device manufacturing. The supervisor leads document control workflows, controlled records, batch record issuance, retention, and audit support. The role strengthens documentation quality and compliance systems that support reliable manufacturing and inspection readiness.

What you'll do

• Oversee Quality Document Control workflow and priorities
• manage development, revision, routing, issuance, review, archival, and retention of controlled documents
• support Master Batch Records and SOPs
• maintain issuance records and logs
• manage change controls and periodic reviews
• support audits
• generate metrics
• uphold Good Documentation Practices and cGMP requirements
• improve processes and workflows.

What we're looking for

Skills & competencies

quality document control supervisor

brighton mi

biovire

quality systems

document control

cgmp

master batch records

sops

audit support

pharmaceutical manufacturing

Work arrangement

• Weekend coverage required

Benefits & perks

• Company-sponsored medical, dental, vision, and life insurance, plus paid time off.

Why this role

Hands-on Quality Systems leadership supporting pharmaceutical and medical device manufacturing as the organization advances toward commercialization.

About the employer

Biovire is hiring for this role. Industry: Instruments and Related Products Manufacturing for Measuring, Displaying, and Controlling Industrial Process Variables. Sector: 33.