Multi Skilled Engineer II

Role Summary The Multi-skilled Maintenance Engineer will be responsible for maintaining specialist pharmaceutical equipment and facility installations to support our manufacturing and QC operations. They will be primarily responsible for equipment breakdown repairs & ongoing maintenance work of manufacturing equipment and associated utility systems. They will plan and complete a range of reactive & planned maintenance works associated within the GMP facility & lab as well as order and maintain critical spares. The role will be shift-based working full-time on a rolling shift pattern of 2 on-2 off, 3 on-2 off, 2 on-3 off. This will rotate across earlies and lates every 14 days. The early shift will start from 0600 AM to 1600 PM; late shift will be from 1100 AM to 2300 PM. Key Responsibilities Responding to & diagnosing faults and repair of equipment breakdowns. Repairing & improving other equipment issues. Ensuring equipment is handed back to production in 100% safe condition. Conducting risk assessment prior to any maintenance work. Completing breakdown & repair reports. Planning and undertaking scheduled maintenance. Creating maintenance procedures (Including writing SOPs). Managing contractors and their activities. Providing support to Facilities, Validation and Capital Project Engineering as required. Managing stocks of critical engineering spares and equipment. Maintaining an engineering workshop. Providing operator training as necessary. Using manuals and failure history to develop preventative tasks. Providing SME support to other business functions. Deputising in other roles as required. Demonstrated skills and competencies E – Essential P – Preferred Experience 3 years of working within a clean room and regulated environment. (P) Working in a Pharmaceutical or other heavily regulated industry. (E) HVAC, compressed gases, and integrated control systems knowledge. (P) Operating within the requirements of a Quality Management system. (E) Project management experience. (P) Equipment validation lifecycle knowledge. (P) Control system (PLC) experience. (E) CMMS experience (E) Experience of managing and performing planned preventive maintenance. (E) Experience in GMP standard quality management systems (i.e. CAPAs, CCs & Deviations) (E) Qualifications Bachelor of Science – Relevant engineering degree or HNC/D with relevant experience. Skills/Specialist knowledge Working with small/medium scale manufacturing and analytical equipment. Pharmaceutical utility systems and controls. BMS and EMS. Clean room operations. Computer literate – Microsoft Office suite. Knowledge and expertise in small scale pharmaceutical manufacturing equipment. (P) Knowledge of current standards, procedures, and controls for GMP cleanroom facilities and equipment. (P) Knowledge and expertise in utility systems from HVAC to medical gases etc. (E) #J-18808-Ljbffr