Katalyst Healthcares & Life Sciences seeks a Sr. Engineer – Process Development (CQV) to lead commissioning, qualification, and validation of automated and semi-automated packaging equipment in a GMP FDP manufacturing environment.
You will author IQ/OQ/PQ protocols, maintain Master Validation Plans, and serve as the technical SME for automated systems, labeling, and packaging validation, collaborating with Engineering, Quality and Manufacturing.
#J-18808-LjbffrSenior CQV Engineer - GMP Automation & Validation in newark at Unknown Company
This position is listed as full time and onsite.