Senior Specialist, QA Operations (Temporary)
Vir Biotechnology · San Francisco, CA
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Role summary
Vir Biotechnology seeks a Senior Specialist for Quality Operations on a temporary 12+ month contract to oversee manufacturing, testing, and packaging compliance at internal facilities and external partners. The role supports cGMP adherence and regulatory requirements across clinical and commercial product development.
What they're looking for
- Bachelor's degree in scientific discipline
- 5+ years quality assurance, operations, or manufacturing experience in GMP environment
- Knowledge of cGMP regulations and quality systems
- Experience with deviations, CAPAs, change controls, and investigations
- Strong organizational and communication skills
- CMO, CTL, or supplier management experience preferred
What you'll be doing
- Oversee quality activities at CMOs, CTLs, and suppliers for manufacturing and testing operations
- Review quality records including deviations, CAPAs, change controls, and validation documentation
- Support batch disposition, release activities, and manufacturing record reviews
- Collaborate with cross-functional teams on quality issues and compliance escalation
- Assist with audits, supplier agreements, and continuous improvement initiatives
Compensation$52.00-$70.00 per hour
Privacy & handoff
This role links to Vir Biotechnology's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.