Role Purpose:We are seeking an experienced Mechanical Engineer to support the Commissioning, Qualification, and Verification (CQV) efforts for the installation and integration of heat pump equipment and two boiler equipment packages on our clients GMP pharmaceutical manufacturing site based in County Waterford.The role will involve close collaboration with project engineering, CQV, quality assurance, and operations teams, focusing on delivering qualified utility systems to support four main operational areas (e.g., production, fill-finish, packaging, warehousing) and ancillary spaces (e.g., labs, maintenance, and utility buildings).Project-based role on an active GMP site with potential for weekend work during key CQV phasesInterface with construction, startup, and operational environmentsMay require field work including equipment inspections and system verificationCore Duties and Responsibilities:CQV & Project SupportLead and support CQV activities for heat pump and boiler systems, including:Design Qualification (DQ) reviewCommissioning protocol generation and execution (FAT, SAT,)Verification of mechanical installation (piping, pumps, exchangers, valves)System walkdowns and punch list resolutionReview and approval of P&IDs, datasheets, isometrics, and turnover packagesEngineering ImplementationReview and contribute to the design and layout of mechanical systemsOversee vendor equipment delivery, installation, and field verificationInterface with building management systems (BMS/EMS) for control and monitoring setupSupport tie-in and integration planning with existing utility networks (steam, hot water, chilled water, etc.)Documentation & ComplianceGenerate and review engineering and CQV documentation per site GMP standards, including:Mechanical Completion documentationUtility Impact AssessmentsRisk assessments and URS traceabilityTurnover package compilation and support handover to OperationsCross-functional CollaborationLiaise with project teams, contractors, vendors, validation, and QA to ensure mechanical systems are installed and qualified per cGMP and safety requirementParticipate in project and CQV meetings, tracking action items to resolutionEducation & Qualifications Required:Bachelor's degree in Mechanical Engineering or related discipline5+ years of experience in mechanical systems implementation on pharmaceutical/biotech facilitiesExperience in CQV for utility systems (preferably boilers, heat pumps, HVAC, chilled/hot water)Strong understanding of GMPs, GEP,Familiarity with ASME B31.3, PED, and relevant mechanical/utilities standardsExcellent problem-solving, communication, and technical writing skillsPrevious experience with green or energy-efficient technology integration (e.g., heatpumps) desired.Ability to read and redline P&IDs, isometrics, and mechanical schematics an advantageUnderstanding of site utility systems and their impact on GMP manufacturing an advantage.For information on how we process your data, please see our Prochem Privacy Policy.