Basic SummaryThe Head of Engineering is responsible for leading all site engineering, maintenance, utilities, facilities, and capital project activities to ensure a safe, compliant, and reliable pharmaceutical manufacturing environment. This role ensures the site meets GMP, HPRA/FDA/EU regulatory expectations, maintains high equipment reliability, delivers strategic capital investment, and implements long-term engineering excellence to support business growth.LocationOnsite at our facility in Loughrea.Key ResponsibilitiesLeadership & StrategyDevelop and execute the site engineering & technical services strategy.Lead engineering teams including maintenance, utilities, calibration, projects, facilities, and automation.Champion safety, reliability, and continuous improvement.Work with value streams to improve OEE & efficiency levels on key production processes.Engineering Governance & ComplianceMaintain GMP-compliant systems and equipment.Upgrade and own engineering policies and standards.Oversee regulatory inspections and statutory compliance.Maintenance & ReliabilityDirect preventive, predictive, and condition-based maintenance.Implement reliability engineering practices.Reduce downtime and equipment-related deviations.Capital Projects & Site ExpansionLead the CAPEX portfolio and major site expansions.Manage design, construction, C&Q, and handover.Control budgets and vendor performance.Support new commercial contract enquiries with CAPEX & operational standards (i.e. machine speeds etc.)Facilities, Utilities & EnergyOversee HVAC, water systems, boilers, chillers, compressed air, and cleanroom utilities.Manage facilities, buildings, grounds, and contractor control.Drive sustainability and energy-saving initiatives.Automation, Controls & DigitalisationOwn the automation strategy.Support MES, data integrity and Industry 4.0 initiatives.Ensure cybersecurity for control systems.Budget, People & PerformanceManage operational and capital budgets.Develop engineering talent and succession plans.Monitor KPIs including OEE and equipment uptime.Education and QualificationsEssential QualificationsDegree in Engineering.10+ years pharmaceutical or GMP-regulated leadership.Strong knowledge of EU GMP, HPRA/FDA requirements.Proven CAPEX and maintenance strategy experience.Desirable QualificationsMaster’s degree or Chartered Engineer.Lean, TPM, Six Sigma experience.Automation and digital transformation exposure.Skills and CompetenciesLeadership and communication skills.Strategic thinker with strong problem‑solving.Excellent stakeholder management.Data‑driven decision‑making.Ability to manage change in a regulated environment.Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non-traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities.
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