Job Description
Job Title: CQV Engineer Location: United States This opportunity is open only to candidates who are currently authorized to work in the United States. Job Summary Seeking experienced CQV Engineers to support a large greenfield biopharmaceutical manufacturing project. Candidates should have strong hands-on experience in commissioning, qualification, startup, and validation activities within GMP-regulated environments. Key Responsibilities Execute commissioning, qualification, and startup activities for GMP equipment and utility systems. Develop and execute IQ/OQ protocols, test plans, and turnover packages. Support startup, troubleshooting, and operational readiness activities. Review P&IDs, vendor documents, and system impact assessments. Coordinate with engineering, automation, validation, quality, and operations teams. Support deviations, change controls, punch list resolution, and compliance activities. Participate in FAT/SAT, walkdowns, and mechanical completion activities. Require...