Cytokinetics
New York, NY
A leading biopharmaceutical company seeks an Associate Director, Clinical Quality Assurance Auditor to lead GCP/GLP/GVP audits and manage the CQA audit program. This role requires a minimum of 10 years in quality compliance within pharma/biotech, alongside a bachelor’s in life sciences. The candidate will oversee audit activities, facilitate inspection readiness, and mentor QA staff, contributing to the quality culture and compliance objectives of the organization. This position offers significant influence in advancing quality standards for clinical trials and may require up to 60% travel.
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