Deviations Investigation Lead — GMP Quality & CAPA
Kindeva Drug Delivery
Kindeva Drug Delivery is seeking a Deviations Investigation Specialist to join our Production Operations – Compliance Investigation group. You will lead deviation investigations, assess root causes, and develop CAPAs in collaboration with Quality, Engineering, and Operations. You will author clear investigation records, perform risk assessments, and ensure compliance with GMP and quality systems while driving continuous improvement across manufacturing processes. #J-18808-Ljbffr Kindeva Drug Delivery
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