Biopharma Validation Engineer - GMP IQ/OQ/PQ Focus

Syner-G is seeking a Validation Engineer to develop and execute validation protocols for multiple processes. You will drive quality performance and regulatory compliance by defining and maintaining the validation program across the organization. The role requires a bachelor’s in a life science and 3–10 years in biotech/pharma/medical devices with FDA cGMP, FMEA, and risk analysis exposure. Candidates should be skilled in writing IQ/OQ/PQ documents and related reports. #J-18808-Ljbffr