A leading global clinical trial services organization is seeking an experienced Associate Director, Tech QA to oversee technology audits and manage Quality Assurance personnel. With 7-10 years of experience in CRO, Pharmaceutical, or Biotechnology and strong knowledge in Computer Systems Validation (CSV), the ideal candidate will ensure compliance with GXP regulations. Additionally, the role requires oversight of internal audits and corrective actions arising from quality events, contributing to overall product integrity and compliance efforts. #J-18808-Ljbffr