Looking to speak with experienced CQV Engineers to plan, prepare, and execute commissioning and qualification activities for clean utilities and equipment at a sterile drug-product manufacturing site. Ensure all work aligns with site standards, global procedures, and regulatory expectations.Key ResponsibilitiesDevelop and execute CQV documentation and testing for clean utilities and GMP equipment, ensuring compliance with site standards and EU/FDA requirements.Drive delivery of CQV scope—safely, on schedule, and with high-quality documentation, including deviation and risk management.Conduct FATs and integrate results into the full qualification lifecycle.Ensure all required training and project records are completed on time.Core CompetenciesProven end-to-end CQV experience across the full project lifecycle.Strong background with sterile manufacturing utilities, including PW/WFI, clean steam, and high-purity gas systems.Effective communicator with strong documentation, planning, and cross-functional teamwork skills.Experience using electronic validation systems (e.g., ValGenesis, Kneat).