Manager, Supplier & Internal Auditor
Vaxcyte · San Carlos, CA
The apply link worked recently (not employer-confirmed).
Role summary
This role supports quality assurance by planning and conducting supplier and internal audits to verify compliance with global regulations, industry standards, and quality systems. The successful candidate will hold audit certification and demonstrate expertise in GMP, GLP, GCP, ICH, and ISO 13485 within pharmaceutical, biotechnology, or medical device settings. Responsibilities include evaluating supplier compliance, coordinating corrective actions, and identifying process improvements across operations.
What they're looking for
- Certified auditor with pharmaceutical, biotechnology, or medical device industry experience
- Strong working knowledge of GMP, GLP, GCP, ICH, and ISO 13485 standards
- Ability to plan, schedule, and conduct on-site and remote audits
- Experience evaluating supplier compliance with regulations and quality requirements
- Cross-functional collaboration skills with technical and regulatory teams
- Proficiency in audit documentation, reporting, and CAPA follow-up processes
What you'll be doing
- Plan and execute supplier audits to assess compliance and support qualification programs
- Conduct internal audits of quality systems and operational processes against regulatory standards
- Develop and maintain risk-based internal audit program scheduling
- Review supplier responses to audit findings and verify corrective action effectiveness
- Document audit observations and support regulatory inspection readiness
Privacy & handoff
This role links to Vaxcyte'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.