Global GCP/GLP QA Director - Inspections & CAPA Lead

A global biotechnology firm seeks an Associate Director/Director for GCP/GLP QA. This role involves maintaining the global clinical/GLP quality management system and leading quality investigations. Candidates should have over 15 years of clinical research experience and at least 10 years in quality management, with strong communication skills in English. An advanced degree is preferred. The position is full-time with responsibilities that include regulatory compliance and optimizing QA procedures. #J-18808-Ljbffr