Job Description
Job Title: Automation Engineer - R&D\n Directorate: Logistics\n Location: Milton Keynes, UK\n Reporting to: Production Supervisor\n Contract Type: Permanent\n Salary: £65,000 per annum + Exceptional Benefits (Health & Wellbeing, Family Support, Time Away, Lifestyle Perks)\n\nAbout the Role\n\nAre you ready to play a key role in shaping the future of automation within a state-of-the-art R&D facility?\n\nWe're looking for an experienced Automation Engineer to join our team in Milton Keynes. As a senior contributor, you'll lead the design and implementation of cutting-edge process control systems-PLC, DCS, HMI, SCADA-for a high-performance, GMP-regulated manufacturing environment.\n\nThis is an exciting opportunity to make a direct impact on the setup and development of a new facility, work on high-value capital projects, and support innovative product introductions with advanced automation solutions.\n\nKey Responsibilities\n\nLead automation engineering on large-scale capital projects from design through validation and startup.\n\nDevelop and maintain control systems using PLC, DCS, HMI, and SCADA technologies.\n\nWrite and review key documentation (URS, SDS, IQ/OQ/PQ, SOPs) and ensure compliance with GAMP and 21 CFR Part 11.\n\nSupport system lifecycle activities, including change control and system upgrades.\n\nTroubleshoot control systems and instrumentation, perform root cause analyses, and recommend improvements.\n\nLead the design, integration, and testing of automation systems for both new and existing process equipment.\n\nCollaborate across departments to support safe, reliable, and compliant operations.\n\nProvide out-of-hours engineering support as needed (rotational/on-call basis).\n\nWhat We're Looking For\n\nEducation & Experience:\n\nBachelor's or Master's in Electrical Engineering, Computer Science, Chemical/Biotech Engineering, or a related discipline.\n\nMinimum 2 years of hands-on experience with Emerson DeltaV (v11+) and Rockwell Automation FactoryTalk / ControlLogix.\n\nProven track record in pharmaceutical or biotech process automation and compliance with cGMP standards.\n\nTechnical Skills:\n\nExpertise in batch control systems, automation software development, and industry standards (ASTM E2500, ISA S88/S95).\n\nExperience with CIP, COP, HVAC, autoclaves, bioreactors, and water systems (RO/WFI).\n\nSkilled in process control documentation, commissioning, and validation.\n\nSoft Skills:\n\nStrong leadership, communication, and technical writing skills.\n\nComfortable working in cross-functional teams and adapting standard principles to complex challenges.\n\nWhy Join Us?\n\nBe part of a pioneering R&D setup with direct influence on design and operations.\n\nThrive in a dynamic, innovation-driven environment with clear opportunities for progression.\n\nEnjoy a competitive salary and a comprehensive benefits package focused on wellbeing, work-life balance, and family care