Pharma Validation Engineer: cGMP Quality & Compliance
Listed on 2026-10-01
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Fresenius Kabi in Grand Island, Nebraska, seeks a Validation Specialist to support qualification activities, equipment testing, and technical support for Operations. You will validate and revalidate systems, document results, and ensure cGMP compliance.
The role involves programming instruments, executing validation studies, preparing Final Reports, and assisting in deviation investigations. Strong attention to detail and teamwork are essential.
The Pharma Validation Engineer: cGMP Quality & Compliance role at Fresenius SE & Co. KGaA is now open for applications in Grand Island, NE, United States.
Are you ready to take on the Pharma Validation Engineer: cGMP Quality & Compliance role at Fresenius SE & Co. KGaA?
We would love to welcome a new Pharma Validation Engineer: cGMP Quality & Compliance to our team in Grand Island, NE, United States.
For the Pharma Validation Engineer: cGMP Quality & Compliance position at Fresenius SE & Co. KGaA, we are reviewing applications now.
(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).