Project Engineer (2 x Contract Roles)Contract Duration: 12-month rolling contractsStart Date: January / February 2026Rate:€45 - €65 per hourLocations:•Westport, Co. Mayo•Sligo, IrelandOverviewWe are seeking experiencedProject Engineersto support capital projects, process improvements, and operational engineering activities across pharmaceutical manufacturing sites. These roles will focus on thedelivery of capital projects, equipment integration, process engineering support, and continuous improvement initiatives, ensuring all projects are executed safely, compliantly, and in line with site objectives.Working closely with Engineering, Production, Quality, Automation, and external partners, the Project Engineers will play a key role in maintaining and improving site capability while delivering new and upgraded manufacturing systems.Key ResponsibilitiesProject & Capital DeliveryManage capital engineering projects from concept through commissioning and handover, including equipment, utilities, and facility upgrades.Develop and manage URS documentation, project plans, feasibility studies, cost estimates, and schedules.Coordinate vendor selection, contractor management, and procurement activities.Lead design reviews, project meetings, and technical decision-making.Ensure compliance with cGMP, EHS, ASME BPE, ISPE guidelines, and site engineering standards.Oversee equipment installation, utilities integration, FAT, SAT, commissioning, and validation activities.Ensure full project documentation, including O&M manuals, training, spare parts, and preventive maintenance plans.Engineering & Operational SupportProvide hands-on engineering support to maximise equipment availability, reliability, and process performance .Troubleshoot manufacturing and process issues in a live production environment.Support automation and control system activities where required.Partner with Production to optimise equipment performance and minimise downtime.Continuous Improvement & Process EngineeringIdentify and deliver process improvement and cost-reduction initiatives .Support process safety projects and site-wide engineering programmes.Drive improvements in equipment performance, process efficiency, and reliability.Collaboration & CommunicationCoordinate and lead cross-functional project teams .Chair regular project and engineering review meetings.Interface with internal stakeholders and external engineering partners.Support site objectives and broader engineering strategies.Equipment & Systems ExposureAseptic and cleanroom systems including autoclaves, RABS, isolators, LAF units, and filling equipmentProcess equipment such as reactors, vessels, compounding skids, pumps, and filter dryersDrug product manufacturing equipment including tablet presses, coaters, blenders, and milling systemsUtilities including HVAC, CIP, and purified water systemsContainment technologies and automation platforms (e.g. DeltaV )RequirementsDegree in Mechanical, Chemical, Process, Electrical, or related Engineering discipline .5+ years' experience in pharmaceutical, biotech, sterile fill-finish, OSD, or API manufacturing environments.Proven experience delivering capital projects from initiation to handover.Strong working knowledge of change control, commissioning, and qualification .Solid understanding of cGMP and regulatory requirements .Hands-on, structured approach to problem-solving in live manufacturing environments.Strong communication skills with the ability to work effectively across multiple disciplines.Eligibility:Only candidates currently based in Ireland with a valid work visa or EU passport will be considered.To discuss this role in more detail, contactCornéat orfor a confidential discussion.