Capricor
San Diego, CA
Capricor Therapeutics is seeking a Quality Auditor to lead and support audits of GMP, QA, and regulatory processes across manufacturing, labs, and supply chain. The role requires 1–2 years of biopharma auditing experience and strong technical writing to document evidence-based findings.
The successful candidate will collaborate with QA, Regulatory, and Manufacturing teams, contribute to CAPA programs, and help ensure inspection readiness for FDA and other regulators. A CQA is preferred.
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