CQV Engineer – Formulation & Component PreparationDuration:February 2026 – January 2027Location:Cruiserath, DublinWorking hours:39 hours per weekOnsite requirements:Fully OnsiteEngagement Type:LTD Company Contractor onlyHourly Rate:€70–80 per hour, depending on experienceLEGAL RIGHT TO WORK:You must have the legal right to work in Ireland. No sponsorship is available.Atrium Global is supporting a leading client within the pharmaceutical industry to appoint a CQV Engineer specialising in Sterile Drug Product manufacturing equipment.Job OverviewYou will be responsible for the development, execution and delivery of CQV testing documentation and activities across formulation and component preparation equipment for a Sterile Drug Product facility. The role is focused on meeting key deliverables for safety, schedule, and quality, ensuring full compliance with applicable GMP, EU and FDA standards.RESPONSIBILITIESDevelop and execute CQV testing documentation for sterile drug product equipment.Deliver on key project milestones for safety, schedule and quality of documentation/electronic records.Ensure all GMP equipment is tested in line with regulatory and company standards.Ensure non-GMP equipment is tested in accordance with project commissioning requirements.Support deviation management for assigned equipment and utilities.Identify and classify CQV risks and generate mitigation action plans.Perform FAT testing and leverage results into the qualification process.Complete all mandatory training within required timelines.REQUIREMENTSProven capability in delivering CQV testing from initiation through to completion.Full CQV project lifecycle experience from design to C&Q and handover.Experience working within a diverse team of CQV professionals/contractors.Strong CQV experience with sterile manufacturing equipment and integrated automation.Specific experience with: Single Use Mixers, TCUs, Utility Panels, Filtration Systems (TFF), Autoclaves, Parts Washers, Powder Handling Equipment (Blenders, Jet Mills).Strong documentation skills, planning capability and a track record of on-time delivery.Excellent communication skills with the ability to influence stakeholders.Experience working within matrix teams to deliver CQV activities.Degree (BSc or equivalent) in a scientific, technical, or engineering discipline.Minimum 5 years pharmaceutical industry experience, ideally with sterile drug product filling line exposure.