Description
The Validation Engineer II will support validation and commissioning activities for equipment, utilities, facilities, and controlled temperature units in a regulated pharmaceutical or biopharmaceutical environment. Responsibilities include developing and executing IQ, OQ, and PQ protocols and reports, temperature mapping, coordinating with cross-functional teams, analyzing validation data, recommending CAPAs, preparing audit documentation, and supporting change controls. The role requires a bachelor’s degree in engineering or a related scientific discipline and 2–6 years of validation experience, with a six-month contract that may extend or convert to full-time.
