CQV EngineerLocation:Dublin, IrelandContract:12-Months (with potential extension)Rate:Competitive – depending on experienceAbout the RoleWe're supporting a leading pharmaceutical company in Dublin who are looking to hire multipleCQV Engineersfor an exciting capital project.These roles will focus primarily onprocess equipment commissioning and qualification, ensuring systems are installed, tested, and verified in line with GMP and project requirements.Key ResponsibilitiesPlan, prepare, and execute CQV documentation (IQ/OQ/PQ) for process equipment and utilities.Support equipment start-up, troubleshooting, and system readiness activities.Review and approve design and vendor documentation.Coordinate with engineering, automation, and validation teams to meet project timelines.Ensure all CQV activities are completed in compliance with GMP and site quality standards.Participate in FAT/SAT execution and system handover.RequirementsMinimum 5 years' experience as a CQV Engineer within the pharmaceutical or biotech industry .Proven experience working on a project through the full lifecycle — from design and installation through to qualification and handover.Strong understanding of process equipment, clean utilities, and GMP requirements.Experience developing and executing commissioning and qualification protocols .Excellent communication and documentation skills.Ability to work independently within a project team environment.Why Apply?Opportunity to work with a top-tier pharma client on a major project.Competitive daily/hourly rate and long-term contract potential.Dublin-based with exposure to cutting-edge process systems.