Katalyst-Healthcares- seeks a Validation Contractor to oversee CQV activities in a regulated pharma/medical device environment. The role ensures facilities, equipment, utilities, and processes meet cGMP and regulatory standards.
Responsibilities include reviewing URS and IQ/OQ/PQ documents, supporting CSV and validation activities, and contributing to audits and KPI reporting. Collaboration across MSAT, Engineering, Manufacturing, and QC is essential.
#J-18808-LjbffrSenior CQV Validation Engineer in raleigh at Unknown Company
This position is listed as contract and onsite.