Quality Systems Lead — Regulatory Readiness & Inspections
Listed on 2026-10-07
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Quality Assurance - QA/QC
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Healthcare
Vir Biotechnology, Inc. seeks an experienced Temporary Associate Director, Quality Systems (12+ month contract) to oversee the Quality Management System as the company advances regulatory submissions and commercialization readiness.
The role is based in San Francisco, onsite three days per week. You will partner with cross-functional teams to drive core Quality Systems, support inspections, and lead continuous improvement while ensuring compliance with FDA, ICH, and global GMP expectations in
We have an opening for a Quality Systems Lead — Regulatory Readiness & Inspections in San Francisco, CA, United States within Bio & Pharmacology & Health, Management & Operations.
Learn more about the Quality Systems Lead — Regulatory Readiness & Inspections role in the description above.
We appreciate your interest in this position.
Join Vir Biotechnology, Inc. and contribute to our ongoing work.
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