Avenzo Therapeutics, Inc. in San Diego, CA or Remote U.S. is seeking an Associate Director, Quality Assurance to lead GMP documentation, QA oversight of contract manufacturers, and CAPA investigations while ensuring compliance with 21 CFR parts and internal procedures.
Reporting to SVP Regulatory Affairs, you will develop and maintain QMS processes, review batch records, manage QTAs, and drive inspection readiness. Travel up to 15% may be required.
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