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 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 & 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 role working full-time basis 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 0600AM to 1600PM; late shift will be from 1100AM to 2300PM. 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. • Provide 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 gasses etc. (E) LI-DNI