Automation Engineer

Summary: Our client, a leading pharmaceutical manufacturing company based in Co. Kerry, is seeking an Automation Engineer to join their Automation Team. The successful candidate will support the operation and optimisation of automation systems within a GMP aseptic manufacturing environment, ensuring equipment reliability, system compliance, and seamless integration across production and utility systems.Responsibilities: Provide automation support for aseptic fill-finish lines and associated manufacturing systems.Diagnose and resolve automation or equipment faults to maintain system reliability and minimise downtime.Lead and support investigations, deviations, and CAPAs relating to automation and equipment issues.Perform root cause analysis and implement effective corrective and preventive actions in line with site quality procedures.Monitor system performance, analyse data, and identify opportunities to enhance efficiency and compliance.Maintain GMP documentation, including configuration records, change controls, and validation reports.Support qualification and validation activities such as FAT, SAT, IQ, and OQ.Ensure integration of control systems (Siemens S7 1200/1500 PLCs, TIA Portal) with MES, utilities, and data historian systems.Collaborate with operations, quality, IT, and engineering teams to maintain compliant and efficient system operation.Assist with OT/IT network configuration, including communication setup and firewall verification.Participate in vendor assessments and contribute to continuous improvement initiatives across automation systems. Qualifications & Experience: Bachelor’s degree in Engineering, Information Systems, or a related discipline.Minimum of 5 years’ experience in an automation or manufacturing support role within the life sciences industry.Knowledge of GMP cleanroom operations and aseptic manufacturing practices.Hands-on experience with Siemens S7 1200/1500 PLCs and Siemens TIA Portal software.Ability to work on electrical and control panels with solid technical understanding.Experience supporting CQV activities and managing automation systems through their lifecycle.Familiarity with ISA-95 and ISA-88 standards.Understanding of OT network design, configuration, and testing.Strong teamwork, communication, and problem-solving skills.Prior experience in aseptic fill-finish or drug product manufacturing environments is advantageous.