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