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.
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.
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.
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).
Job Title: PLC Automation EngineerLocation: Dundalk Ireland Industry: Pharmaceutical / Life SciencesRole OverviewThe PLC Automation Engineer will support the design development commissioning and lifecycle management of automated systems within a GMP-regulated pharmaceutical manufacturing environment...
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.
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.
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.
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).
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