Summary: Ourclient, a leading pharmaceuticalmanufacturer in Co. Kerry, is seekingan Automation Engineerto join their Automation Team. The successful candidate will support the operation, maintenance, and optimisation of automated systems within an aseptic GMP environment, ensuring system reliability, compliance, and efficient manufacturing performance. Responsibilities: Provideautomationengineeringsupporttositecapitalprojects Provide daily automation support for asepticfill-finish, manufacturingandfacilities operations. Troubleshootandresolvecontrolsystemandequipmentissuestominimisedowntime. Support investigations, deviations, and CAPAs, including root cause analysis and documentation. Maintain andupdate validatedcontrolsystems(Siemens S7, TIAPortal,GE iFix,) and related networks. Ensure automation systems remain compliant with cGMP, data integrity, and site procedures. Supportqualificationandvalidationactivities,includingFAT,SAT,IQ,andOQ. CollaboratewithEngineering,Quality,andOperationstomaintainsystem performance and ensure smooth production execution. Contribute to continuous improvementprojects to enhance reliability,efficiency, and compliance. Support training and knowledge sharing across manufacturing and maintenance teams. Interfacewithexternalvendorsprovidingsupportforplantandequipment. Qualifications & Experience: BachelorsdegreeinElectrical,Electronic,Automation,orrelatedEngineering discipline. Minimum of 5 years automation or manufacturing support experience in a GMP pharmaceutical or biopharmaceutical environment. Hands-onexperiencewithSiemensS7(Step7/TIAPortal)andGEiFixsystems. Knowledgeofelectricalcontrolsystemsandschematics. Knowledge of automation lifecycle, validation, and data integrity(GAMP 5, Annex 11, FDA 21 CFR Part 11). Familiaritywithasepticprocessingandcleanroomoperations. Strong problem-solving, analytical, and communication skills.