Job Specification – Trade Qualified Mechanical Fitter
Location: Dublin, Ireland
Job Purpose
The Mechanical Fitter is responsible for the maintenance, troubleshooting, repair, installation, and continuous improvement of mechanical systems and production equipment within a GMP-regulated pharmaceutical manufacturing environment. The successful candidate will ensure equipment reliability, minimise downtime, and support safe and compliant operations across the facility.
Key Responsibilities
Carry out planned preventative maintenance (PPM) on manufacturing and utility equipment.
Diagnose and repair mechanical faults on production machinery and plant systems.
Install, commission, and validate new mechanical equipment and process lines.
Support breakdown response activities to minimise operational downtime.
Read and interpret engineering drawings, P&IDs, schematics, and technical manuals.
Perform alignment, fitting, welding, pipefitting, and fabrication activities as required.
Ensure all maintenance work is completed in accordance with GMP, health & safety, and company procedures.
Maintain accurate maintenance documentation and records using CMMS systems.
Participate in root cause analysis and continuous improvement initiatives.
Liaise with production, quality, and engineering teams to support operational targets.
Assist contractors and external service providers during site works and shutdown activities.
Adhere to all EHS policies, permit‑to‑work systems, and safe systems of work.
Candidate Requirements
Essential Qualifications & Experience
Trade qualification in Mechanical Fitting, Maintenance Fitting, or related mechanical discipline.
Minimum 3–5 years’ experience in an industrial manufacturing environment.
Experience working within pharmaceutical, biotechnology, food, or other regulated industries preferred.
Strong knowledge of pumps, valves, conveyors, compressors, gearboxes, and rotating equipment.
Experience with preventative maintenance systems and fault finding.
Ability to read and interpret technical drawings and documentation.
Strong understanding of GMP and safety standards.
Excellent troubleshooting and problem‑solving skills.
Good communication and teamwork abilities.
Flexible approach to shift work, call‑outs, and overtime where required.
Experience in cleanroom or sterile manufacturing environments.
Welding and fabrication experience.
Familiarity with CMMS systems such as SAP, Maximo, or similar.
Working knowledge of Lean Manufacturing or continuous improvement methodologies.
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