Summary
Our client, a leading pharmaceutical manufacturer in Co. Kerry, is seeking an Automation Engineer to 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
Provide automation engineering support to site capital projects
Provide daily automation support for aseptic fill‑finish, manufacturing and facilities operations.
Troubleshoot and resolve control system and equipment issues to minimise downtime.
Support investigations, deviations, and CAPAs, including root cause analysis and documentation.
Maintain and update validated control systems (Siemens S7, TIA Portal, GE iFix) and related networks.
Ensure automation systems remain compliant with cGMP, data integrity, and site procedures.
Support qualification and validation activities, including FAT, SAT, IQ, and OQ.
Collaborate with Engineering, Quality, and Operations to maintain system performance and ensure smooth production execution.
Contribute to continuous improvement projects to enhance reliability, efficiency, and compliance.
Support training and knowledge sharing across manufacturing and maintenance teams.
Interface with external vendors providing support for plant and equipment.
Qualifications & Experience
Bachelor’s degree in Electrical, Electronic, Automation, or related Engineering discipline.
Minimum of 5 years’ automation or manufacturing support experience in a GMP pharmaceutical or biopharmaceutical environment.
Hands‑on experience with Siemens S7 (Step 7 / TIA Portal) and GE iFix systems.
Knowledge of electrical control systems and schematics.
Knowledge of automation lifecycle, validation, and data integrity (GAMP 5, Annex 11, FDA 21 CFR Part 11).
Familiarity with aseptic processing and cleanroom operations.
Strong problem‑solving, analytical, and communication skills.
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