Senior Facilities Engineer - excellent opportunity in Medical Devices manufacturing in Limerick. Candidates with 5 yrs experience of Facilities and Maintenance Engineering in a GMP please apply.Apply today Role:Description:ResponsibilitiesSupport the Utilities Manager in the Ops readiness tasks for the Facility department responsibilities on the IPA and PG Tank Farm.Ongoing preparation and review of technical and operational documentation and procedures applicable to ensuring sustainable delivery of Utility and facility services to the product production.Creates/modified designs for intermediate problems.Designs/modifies complex components/processes.writes detailed design specifications.Safety management of maintenance contractors – Utilise the permit to work systems. Review RA MS documents.Ongoing review and updating of CMMS procedures with a focus on system readiness and resource availability.Grasps complexities and sees relationships amongst dataDetermines consequences and alternatives; makes recommendationsSupport resource estimates and coordination needed (materials, budget, time and people) to accomplish assigned individual tasks.Anticipates future directions. Benchmarks internally and externally. Recognizes changes in the environment and present resources as indicators of future problems and opportunitiesPlan/conduct small- to medium-size assigned projects within FM engineering requiring conventional types of plans, investigations, and/or equipmentCoordinates and monitor activities associated with projects under the relevant scope of the roleLiaise with the various stakeholders on the Project team and the overall project to ensure clear communication between all partiesReview and approve project documentation, ensuring technical accuracy and adherence to GMP standards.Supporting the generation of key deliverables (in a phase appropriate compliance manner) including system impact assessments, criticality assessments, risk assessments, user requirements specifications, function specifications, design specificationPrepare and execute FAT / SAT and IQ protocols for facilities equipment.Develop training materials and deliver training to technicians / operators.Responsible for compliance with applicable policies and proceduresEncourage compliance with all company Safety, Environmental and Quality systemsAssist in investigations and root cause analysis of process equipment, utility systems and control system anomalies, as well as safety incidents.Ensure that value engineering, constructability reviews and similar processes are effectively utilized to minimize capital expenditures and maximize functional value.Initiate, support and execute continuous improvement activities in safety, energy efficiency, waste elimination across functional areas (production, utilities, logistics, maintenance etc) using lean manufacturing principlesConfirm vendor documentation and executions are compliant prior to service deliverySupport internal and external regulatory audits preparations and follow on requirementsEducation & Experience• Bachelor's degree in chemical engineering or related program with the following years in relevant experience:• 5+ years' experience of working within Engineering in a regulated GMP/Biotech/Med Device environment.• Understanding of CMMS/Asset management strategies and applications• Excellent interpersonal and communication skills with leadership abilities.• Experience on ATEX rated sites is a distinct advantage.• Familiarity with Automated equipment and Automation systems plus supporting systems – SCADA / Historians