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
📌 QA Specialist: Investigations, CAPAs (España)
🏢 Chemo
📍 España
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