Arcadis are seeking a Maintenance Engineer for a Biotech company in Cork. The position is offered on an hourly-rate, 12 month rolling basis.
Position Summary
Our client, a leading biopharmaceutical manufacturing organisation based in Cork, is seeking an experienced Maintenance Engineer to support the reliability, availability, and performance of manufacturing and utility systems within a GMP-regulated environment.
The successful candidate will play a key role in maintaining critical production equipment, utilities, and facility assets while ensuring compliance with regulatory requirements, safety standards, and site maintenance procedures. The role requires hands‑on maintenance experience along with exposure to a Computerised Maintenance Management System (CMMS) for planning, scheduling, execution, and documentation of maintenance activities.
Key Responsibilities
Maintenance & Reliability
- Support the maintenance and reliability of manufacturing equipment and plant utilities.
- Execute and oversee preventative maintenance (PM), corrective maintenance, and predictive maintenance programmes.
- Troubleshoot equipment failures and implement effective root cause solutions.
- Support equipment uptime and minimise production downtime through proactive maintenance strategies.
- Participate in breakdown investigations and implementation of corrective and preventive actions (CAPAs).
- Assist in equipment lifecycle management and asset replacement planning.
CMMS Management
- Utilise the site's CMMS (e.g., SAP PM, Maximo, PEMAC, Oracle, Infor EAM) to:
- Record maintenance histories.
- Maintain asset records.
- Monitor maintenance KPIs.
- Generate maintenance reports and metrics.
- Ensure maintenance documentation within the CMMS is accurate, complete, and GMP compliant.
- Drive continuous improvement of CMMS data quality and asset management practices.
Utilities & Facilities Support
Support maintenance activities associated with some of the following systems:
- Clean Utilities
- Purified Water (PW)
- Clean Steam
- Process Gases
- HVAC Systems
- Cooling Water Systems
- Compressed Air Systems
- Boilers
- Manufacturing Equipment
- Bioreactors
- Media Preparation Systems
- CIP/SIP Systems
- Filtration Systems
- Filling Equipment
- Packaging Equipment
GMP Compliance
- Ensure all maintenance activities are performed in accordance with GMP, EHS, and site quality requirements.
- Support deviation investigations and change control activities.
- Review and approve maintenance documentation as required.
- Participate in audits and inspections, providing maintenance-related support and documentation.
- Ensure calibration and maintenance activities comply with regulatory expectations.
- Identify opportunities for reliability and maintenance process improvements.
- Participate in Lean, Six Sigma, and operational excellence initiatives.
- Support implementation of predictive maintenance technologies and condition monitoring programmes.
- Contribute to maintenance KPI reviews and site reliability initiatives.
Qualifications
- Degree in Mechanical Engineering, Electrical Engineering, Automation Engineering, Manufacturing Engineering, or related discipline.
- Minimum 3+ years' maintenance engineering experience within a pharmaceutical, biopharmaceutical, medical device, or regulated manufacturing environment.
- Experience working within a GMP-regulated facility.
- Hands on experience with a CMMS system.
- Knowledge of preventative and predictive maintenance methodologies.
- Strong troubleshooting and root cause analysis skills.
- Experience in the pharma sector
- Knowledge of clean utilities and facility systems.
- Familiarity with calibration programmes.
- Experience with SAP PM, Maximo, PEMAC, Oracle, or similar CMMS platforms.
- Reliability-centred maintenance (RCM) experience.