Pharma Quality Engineer: Deviation, CAPA & Validation
Listed on 2026-10-07
-
Quality Assurance - QA/QC
Quality Engineering -
Pharmaceutical
Quality Engineering, Pharma Engineer
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
Consider building your career as a Pharma Quality Engineer:
Deviation, CAPA & Validation at Katalyst CRO.
We are seeking a motivated Pharma Quality Engineer:
Deviation, CAPA & Validation to join Katalyst CRO in Illinois City, IL, United States.
The Pharma Quality Engineer:
Deviation, CAPA & Validation position in the Bio & Pharmacology & Health, Engineering field is open for applications.
We have an opening for a Pharma Quality Engineer:
Deviation, CAPA & Validation in Illinois City, IL, United States within Bio & Pharmacology & Health, Engineering.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).