Katalyst CRO is seeking a detail-oriented Quality Engineer with hands-on experience in the pharmaceutical industry to support quality engineering activities across manufacturing and laboratory operations. The ideal candidate will manage deviations, CAPA, change control, and validation, review batch records and SOPs, and ensure GMP, cGMP, and GLP compliance.
You will collaborate with QA, QC, Manufacturing, Validation and Engineering teams to drive continuous improvement and maintain compliant
#J-18808-LjbffrPharma Quality Engineer: Deviation, CAPA & Validation in illinois city at Unknown Company
This position is listed as full time and onsite.