This job is with Autolus Therapeutics, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. Role Summary The Engineering Manager will be responsible for maintaining specialist pharmaceutical equipment and facility installations to support our manufacturing and QC operations. They will be primarily responsible for the shift team supporting equipment breakdown repairs & on-going 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. Key Responsibilities Leadership of a multiskilled engineering team. Own and actively progress teams work load and professional development. Responding to fast paced and complex equipment needs. Lead and structure problem solving to diagnose faults and repair of equipment breakdowns. Foster continuous improvement mind set, focus on root cause, elimination actions. Represent Engineering Dept at multi departmental meetings. Work with equipment suppliers planning for and during major maintenance activities Ensuring equipment is handed back to production in 100% safe condition. Conducting risk assessment prior to any maintenance work. Verifying GDP, ALCOA, GMP and GEP practices are followed in CMMS Creating maintenance procedures (Including writing SOPs). Managing contractors and their activities. Providing support to Facilities, Validation and Capital Project Engineering as required. Provide SME support to other business functions. Demonstrated skills and competencies E – Essential P – Preferred Experience Team leadership experience (E) 3 years of working within a clean room or 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 gasses etc. (E) LI-DNI