CQV Equipment Engineer – Utilities (Sterile Drug Product Facility)Location:DublinSector: Biopharmaceutical | Commissioning & QualificationType: Contract| On-SiteWe are currently seeking a CQV Equipment Engineer – Utilities to join a high-performing team at a leading pharmaceutical facility in Dublin. This role focuses on the commissioning and qualification of utility systems within a state-of-the-art Sterile Drug Product (SDP) facility.Key Responsibilities:Prepare and execute CQV protocols for black utilities (e.g., compressed air, plant steam, chilled water, process waste)Ensure all utilities are tested in compliance with GMP, EU/FDA regulations, and internal proceduresSupport FATs/SATs, field inspections, and system walkdownsManage deviations and implement risk-based CQV strategiesCollaborate closely with vendors, site stakeholders, and contractorsDeliver documentation and training in line with project timelines and quality standardsWhat We’re Looking For:Degree in Engineering, Science, or a related technical field5+ years' experience in pharmaceutical CQV with a focus on utility systemsProven experience across the full CQV lifecycle, from design through handoverStrong understanding of integrated automation in sterile manufacturing environmentsExcellent communication, planning, and documentation skillsThis is an excellent opportunity to work on cutting-edge projects in a global pharmaceutical environment, contributing directly to the launch-readiness of key manufacturing systems. To apply, please send your CV to jobs@forcerecruitment.com
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