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On-site in Dundalk·Full-time·Added 9 months ago (last checked 23 Oct)
17 open roles
Our summary
- Work mode
- On-site, Dundalk
- Contract
- Full-time


Skills
Nice to have
Requirements
What we're looking for
Required Skills & Experience
- Degree in Automation Engineering, Electrical Engineering, Instrumentation, or related discipline.
- Proven experience as a PLC Automation Engineer in a pharmaceutical, biotech, or regulated manufacturing environment.
- Strong hands-on experience with PLC programming, ideally Allen-Bradley / Rockwell systems.
- Experience with SCADA/HMI systems and industrial networks (Ethernet/IP, Profinet, Modbus).
- Solid understanding of GMP environments, regulated change management, and validation principles.
- Ability to read and interpret P&IDs, control narratives, and electrical schematics.
- Experience supporting FAT, SAT, commissioning, and start-up activities.
- Strong troubleshooting, analytical, and problem-solving skills.
- Excellent communication skills and ability to work effectively within cross-functional teams.
Nice to have
Desirable / Nice-to-Have
- Experience with DeltaV, PCS7, or DCS systems.
- Exposure to CSV documentation (URS, FS, IQ, OQ, traceability matrices).
- Knowledge of process equipment automation (bioreactors, CIP/SIP, fillers, packaging).
- Experience working on Irish or EU pharma sites.
- Familiarity with alarm management standards (ISA-18.2 / EEMUA 191).
The role
Job Title: PLC Automation Engineer
Location: Dundalk, Ireland
Industry: Pharmaceutical / Life Sciences
Role Overview
The PLC Automation Engineer will support the design, development, commissioning, and lifecycle management of automated systems within a GMP-regulated pharmaceutical manufacturing environment. The role involves hands-on PLC programming, system integration, troubleshooting, and collaboration with cross-functional teams to ensure safe, compliant, and reliable operation of production and utility systems.
What you'll do
Key Responsibilities
- Design, develop, modify, and maintain PLC control systems supporting pharmaceutical manufacturing, packaging, utilities, and process equipment.
- Program and troubleshoot PLCs (e.g. Rockwell Allen-Bradley, Siemens, Schneider), including development of ladder logic, function block diagrams, and structured text as applicable.
- Support automation commissioning activities, including FAT, SAT, and on-site start-up, ensuring systems meet functional and GMP requirements.
- Interface PLC systems with SCADA/HMI platforms (e.g. FactoryTalk, WinCC, iFIX), ensuring clear operator interfaces and alarm management.
- Interpret and work from P&IDs, control philosophies, functional specifications, and electrical drawings.
- Provide automation support for manufacturing equipment, process skids, packaging lines, utilities (HVAC, WFI, clean steam), and ancillary systems.
- Participate in change control, deviation investigations, and root cause analysis related to automation systems.
- Support Computer System Validation (CSV) activities, including IQ/OQ testing, protocol execution, traceability, and documentation reviews in line with GAMP 5.
- Ensure automation systems comply with GMP, data integrity (ALCOA+), and site quality standards.
- Collaborate with Engineering, QA, Manufacturing, Maintenance, IT, and external vendors to deliver projects and resolve technical issues.
- Provide ongoing troubleshooting and operational support to minimise downtime and improve system reliability.
- Contribute to continuous improvement initiatives, standardisation, and automation best practices across the site.
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