Maintenance Engineer

OverviewPE Global is recruiting for a Maintenance Engineer for our medical device client in Limerick.This is an initial 6-month contract, onsite role.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.Predicts patterns/trends.Grasps complexities and sees relationships amongst data.Determines consequences and alternatives; makes recommendations.Support 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 opportunities.Plan/conduct small- to medium-size assigned projects within FM engineering requiring conventional types of plans, investigations, and/or equipment.Coordinates and monitor activities associated with projects under the relevant scope of the role.Liaise with the various stakeholders on the Project team and the overall project to ensure clear communication between all parties.Review 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 specificationsPrepare 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 procedures.Encourage compliance with all company Safety, Environmental and Quality systems.Assist 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 principles.Confirm vendor documentation and executions are compliant prior to service delivery.Support internal and external regulatory audits preparations and follow on requirements.Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.Education & ExperienceBachelor's degree in chemical engineering or related program with the following years in relevant experience.3+ 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.ContactInterested candidates should submit an updated CV.Please click the link below to apply, call Paul Wheatley on ************ or alternatively send an up-to-date CV to *********Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***#J-*****-Ljbffr