Validation Engineer

CQV Engineer - Greenfield Biopharma ProjectLocation: Holly springs, NCPay: $45-50/hr on W2Job SummaryWe are seeking experienced CQV Engineers for a large-scale greenfield biopharmaceutical manufacturing project in North Carolina. The ideal candidates will have strong hands-on commissioning, qualification, and validation experience supporting upstream/downstream process equipment and critical utility systems within GMP-regulated environments.Candidates should be capable of working independently with minimal supervision and collaborating effectively with cross-functional engineering, manufacturing, and quality teams during facility startup and operational readiness activities.Key ResponsibilitiesExecute commissioning, qualification, and startup activities for GMP manufacturing equipment and utility systems.Develop and execute IQ/OQ protocols, commissioning test plans, and system turnover packages.Support startup and troubleshooting of process equipment and clean utility systems.Coordinate with engineering, automation, validation, and operations teams during project execution.Review P&IDs, design documents, vendor packages, and system impact assessments.Ensure compliance with GMP, GDP, and regulatory requirements.Support deviation investigations, punch list resolution, and change control activities.Participate in walkdowns, FAT/SAT activities, and mechanical completion verification.Drive schedule adherence while supporting aggressive project timelines.Required Experience5+ years of CQV/Startup experience in pharmaceutical, biotech, or life sciences industries.Strong experience in greenfield facility projects.Experience supporting critical utilities including:WFIClean SteamHVACCompressed AirPurified WaterCIP/SIP systemsExperience with upstream and downstream process equipment.Ability to independently execute qualification and startup activities.Strong GMP documentation and protocol execution experience.Excellent communication and coordination skills.Preferred QualificationsExperience with DeltaV, Rockwell, or other automation systems.Prior experience with biologics or sterile manufacturing facilities.Familiarity with Kneat, ValGenesis, or electronic validation systems.Bachelor's degree in Engineering or related technical discipline.

Created: 2026-05-17