Summary : We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment. This is a fast-paced opportunity focused purely on execution of validation protocols-ideal for professionals who thrive on the manufacturing floor. Roles & Responsibilities: Execute IQ/OQ protocols for process equipment Perform equipment walkdowns and verify against design Support SIP/CIP cycles, wet testing, and temperature mapping Work with downstream equipment (ch