This is a great opportunity for an engineer who enjoys working at the intersection of maintenance, systems, and data, and wants to play a key role in keeping a high-performing pharmaceutical manufacturing site running reliably and compliantly.
Key Responsibilities
- Act as technical subject matter expert for MRO processes and systems
- Own and optimise CMMS (SAP-PM) usage in line with global and site standards
- Support maintenance planning and scheduling across GMP production areas
- Create and maintain master data including spare parts, BOMs, and material records
- Manage spare parts lifecycle and obsolescence
- Produce advanced MRO reports and analytics using SAP, Excel, and digital tools
- Support change control, deviation management, documentation retention, and training processes
- Ensure compliance with cGMP, EHS, and corporate governance requirements
- Prepare and present maintenance system data in daily tier meetings
- Perform root cause analysis (FMEA, 5 Whys, Fishbone) and implement CAPA actions
- Coordinate with engineering, global maintenance teams, and site stakeholders
- Drive continuous improvement and standardisation of maintenance practices
Education
- Degree or diploma in Mechanical Engineering, Electrical Engineering, Mechatronics, Industrial Engineering, or similar technical discipline
- Alternatively: Technical apprenticeship + extensive maintenance/MRO experience
- Training in GMP / regulated manufacturing highly desirable
For a confidential discussion and more information on the role, please contact Kevin Griffin.
kevin.griffin@collinsmcnicholas.ie
(021) 2427108
