OverviewAn Automation Engineer is required to support the day-to-day operation and continuous improvement of complex automated manufacturing systems within a large-scale, GMP-regulated aseptic production facility.The role supports automated systems across drug product manufacturing operations, including formulation, aseptic filling, lyophilisation, inspection, and packaging. You will work as part of a multidisciplinary engineering team, ensuring automation systems remain compliant, reliable, and fit for purpose, while also contributing to ongoing improvement and technology upgrades.The environment promotes continuous improvement, innovation, and operational excellence, with a strong focus on patient safety and supply continuity.Key ResponsibilitiesSafety & CompliancePromote a safe working environment by adhering to all EHS, GMP, and regulatory requirements.Ensure automation systems operate and are maintained in a validated state.Automation System OwnershipAct as System Owner for assigned automation platforms within a regulated manufacturing environment.Support the lifecycle management of automation systems, including upgrades, changes, and obsolescence management.Lead and support incident investigations and troubleshooting related to manufacturing automation systems.Provide technical input to deviation investigations and root cause analyses.Implement corrective and preventive actions (CAPAs), including software changes, configuration updates, and documentation revisions.Update design documentation, system descriptions, and SOPs as required.Engineering & InnovationReview existing automation architectures and recommend improvements aligned with current technology and regulatory standards.Support the introduction of new products, processes, and technologies, including engineering assessments, system modifications, and engineering trial runs.Qualifications & ExperienceBachelor’s degree in Electrical Engineering, Automation, Computer Science, Chemical Engineering, Biotechnology, or a related engineering discipline.5+ years’ experience supporting automation systems in an operational manufacturing environment.Strong background in automation design, programming, commissioning, and lifecycle support.Experience working within GMP-regulated environments, including system validation and change management.Proven ability to troubleshoot PLC, HMI, SCADA, serialisation, and vision systems.Automation Technologies (experience in some or all):HMIs: Siemens and Rockwell-based systemsSCADA: iFix, InTouch, Zenon, PCSS7, FactoryTalk ViewFieldbus & Networks: ControlNet, DeviceNet, Profibus, Profinet, AS-i, BACnetManufacturing Exposure (advantageous):Biopharmaceutical formulation and fill/finishAseptic processing and lyophilisationInspection and packaging systemsRegulatory & Standards KnowledgeUnderstanding of GAMP 5, automation software development lifecycleFamiliarity with ANSI/ISA-88 (Batch) and ANSI/ISA-95 (Manufacturing Integration) standardsExperience supporting validated systems in line with regulatory expectationsWhat’s on OfferLong-term role supporting critical manufacturing operationsExposure to complex, high-availability automation systemsOpportunity to contribute to technology upgrades and continuous improvementCollaborative engineering environment with strong technical ownership
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