Position OverviewFacilities Engineer – Permanent role, 100% on-site, Monday to Friday. Location: Stamullen, County Meath.ResponsibilitiesConsult with Engineering team on maintenance requirements and preventative maintenance work.Troubleshoot facilities issues.Manage and maintain all facilities, utilities, equipment, and grounds.Review and develop plant upgrade and modification proposals.Contribute to the maintenance system for the Facilities Engineering Group.Ensure all building repairs and upgrades meet pharmaceutical standards.Maintain facilities documentation in compliance with GMP guidelines.Manage contracts for utilities, security, cleaning, pest control, landscaping, fire protection, security alarms, cameras, access control, garments, and waste management.Control Facility Engineering contractors, including pre‑qualification, site entry, induction, permit to work, method statements, LOTO, inspections, and exit from site.Identify and implement measures to reduce energy costs.Update SOPs, documentation, and technical papers.Implement recycling initiatives.Liaise with the Facilities Engineering team to ensure plant‑related duties are completed successfully.Lead continuous improvement initiatives (TPM, Lean, Six Sigma, Shingo).Assist or lead technical improvements under the department’s continuous improvement program.Demonstrate excellent communication and assertiveness skills with mindfulness.Plan and manage small to medium capital projects to successful completion.Work closely with the H&S Department to meet environmental and safety requirements.Perform validations of various facility systems.Manage maintenance/facility budgets.Coordinate remedial actions identified in audits.Collaborate with PCI Engineering teams on facility projects.Provide technical support for new product introduction and transfers.Manage documentation issues arising from engineering activities.Work with equipment vendors to resolve performance issues.Define, control, and document engineering operation practices.Conduct risk and gap assessments for new or modified equipment.Lead and attend daily handover meetings.Organise and supervise outside contractors (calibration, service contracts, cleaning).Maintain high standards of cleanliness, hygiene, and GMP compliance.Undertake additional tasks assigned by the Engineering Director or Facilities Manager.Set clear goals, communicate them, and ensure progress to completion meeting defined targets.RequirementsDegree in Engineering (mechanical or electrical) is essential.At least 2-5 years of experience in a similar role within GMP‑regulated manufacturing; audit experience desirable.Experience with facilities equipment best‑practice maintenance, CMMS and RCM.Background in continuous improvement and lean production/engineering techniques.Excellent written and verbal communication and documentation skills.Collaborative and able to work independently with minimal direction.Proficient in financial/budgeting skills.Basic working knowledge of Microsoft Office and AutoCAD is an advantage.Equal Employment Opportunity StatementPCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, equity and inclusion are at the core of our company’s purpose: Together, delivering life‑changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity at every level.
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