Job title: cqv engineerthis position is open exclusively to people who are eligible to work in usalocation : united statesjob summary:we are looking for a highly experienced cqv engineer to support a leading cdmo client.this role requires strong hands-on expertise in commissioning, qualification, and validation activities within a pharmaceutical manufacturing environment.key responsibilitiesdevelop and execute cqv documentation for large-scale manufacturing equipmentsupport commissioning, qualification, and validation (iq/oq/pq) activitieswork closely with cross-functional teams including engineering, quality, and operationsensure compliance with gmp and regulatory requirementssupport equipment startup, troubleshooting, and performance verification key requirements10+ years of experience in pharmaceutical industry (no biotech or medical device)strong experience with document development and executionhands-on expertise with fill/finish lines and lyophilizersexperience working in pharma manufacturing environments (cdmo experience preferred) preferredprior experience supporting large-scale manufacturing projectsstrong understanding of gmp, validation lifecycle, and compliance standards