The Project Engineer will support the delivery of capital and site-based projects within a highly regulated pharmaceutical manufacturing environment, with a strong focus onclean utility systems and production support infrastructure. This role is suited to anintermediate-level engineerwho has developed a solid foundation in GMP environments and is now seeking to broaden their experience acrossutilities, process support systems, and equipment projects.Key ResponsibilitiesProject Delivery & CoordinationSupport the execution of equipment, facility, and clean utility projects from concept and detailed design through installation, commissioning, and final handover.Assist with upgrades and modifications to clean utilities including WFI, Purified Water, Clean Steam, Clean Compressed Air, process gases, CIP systems, and supporting infrastructure.Support projects involving production and support equipment such as vessels, skid-mounted systems, HVAC, chillers, and building services.Coordinate activities with Engineering, Operations, Quality, Automation, and external vendors to ensure project milestones are achieved.Documentation & GMP CompliancePrepare, review, and maintain project documentation including URS, functional/design specifications, commissioning plans, test scripts, and handover packages .Ensure project activities are executed in accordance with GMP, FDA, and internal quality standards, supporting audit and inspection readiness.Participate in risk assessments, impact assessments, and change control activities throughout the project lifecycle.Commissioning, Start-Up & TroubleshootingActively support commissioning and qualification activities for clean utilities, process support systems, and equipment.Execute commissioning test scripts, document results, and support system start-up activities.Assist in troubleshooting issues encountered during commissioning, qualification, or early operational phases, working closely with vendors and site SMEs.Support deviation resolution, punch-list closeout, and transition to operations.Experience & Qualifications3–5 years' engineering experience within a GMP-regulated pharmaceutical or life sciences environment .Hands-on experience supporting clean utilities, facilities, or process support systems (e.g. WFI, PW, Clean Steam, HVAC, CIP).Working knowledge of project lifecycle phases including requirements definition, design, installation, commissioning, and handover.Experience preparing and maintaining technical and GMP documentation such as URS, test plans, commissioning reports, and as-built documentation .Exposure to validation, qualification, and investigation processes is highly advantageous.Skills & CompetenciesStrong organisational skills with the ability to manage multiple workstreams and priorities.Practical, hands-on approach to problem solving, particularly during commissioning and start-up phases.Sound understanding of GMP and FDA regulatory requirements as they apply to utilities and manufacturing systems.Effective communicator, capable of working cross-functionally with Engineering, Manufacturing, Quality, and external contractors.High attention to detail, with a strong focus on safety, quality, and compliance.Ability to work independently while contributing effectively within a project team.Desirable QualificationsDegree in Mechanical, Electrical, Process, Chemical, or related engineering discipline.Experience working on clean utility or aseptic manufacturing projects