LEONFARMA in León is seeking a QA Specialist (PRD) to oversee production-related quality activities in a GMP manufacturing environment.
You will lead investigations, approve CAPA plans and change controls, and provide real-time QA support on the shop floor.
The role requires at least 3 years of experience in pharmaceutical QA and a strong focus on quality compliance, continuous improvement, and collaboration across Operations, Engineering and Quality Control. #J-18808-Ljbffr