Overview
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.
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