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.
#J-18808-LjbffrPharma Validation Engineer: cGMP Quality & Compliance in northern at Unknown Company
This position is listed as full time and onsite.