The role leads validation activities, change control, deviations, CAPA and risk management, working with Technical Operations to ensure compliance with CFR/ICH and internal standards. 8+ years in GMP QA and a Life Sciences degree are required, Master’s preferred. Travel 10-25%.
#J-18808-LjbffrAssociate Director, QA – GMP & Validation (Remote) in denver at Unknown Company
This position is listed as full time and onsite.