Biopharma QA Auditor | Compliance SME; Hybrid
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Avid Bioservices in United States, California, is seeking an individual contributor to oversee audits, data reviews, and regulatory compliance activities integral to cGMP practices. You will prepare audit reports, coordinate corrective actions, and support supplier quality with metrics and SOP updates.
The role emphasizes ongoing QA expertise, SOP creation, and collaboration with cross‑functional teams to uphold regulatory standards and patient safety.
This opportunity is for the Biopharma QA Auditor | Compliance SME (Hybrid) role at Avid Bioservices.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Tustin, CA, United States.
This opportunity is part of our work in Finance.
The advertised compensation is 103..
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