PE Global is recruiting for a Maintenance Engineer for our medical device client in Limerick. This is an initial 6-month contract, onsite role.
Responsibilities
• Support 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 specifications
• Prepare 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 & Experience
• Bachelor'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.
Interested 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***