We are seeking enthusiastic Graduate or Junior Automation Engineers with exposure to GMP-regulated environments to join our clients high-performing engineering team in Ballydine Co. Tipperary. This is an excellent opportunity for early-career engineers to develop hands-on automation expertise within a world-class pharmaceutical manufacturing site.
You will work alongside experienced Automation and Process Engineers supporting projects focused on manufacturing systems process controls data integrity and equipment automation within a highly regulated environment.
Key Responsibilities
Support automation activities across manufacturing utilities and laboratory equipment within a GMP environment.
Assist in configuring testing and troubleshooting automation systems (e.g. PLC SCADA DCS systemsAllen Bradley Siemens DeltaV).
Participate in commissioning qualification and validation activities (IQ OQ PQ) for automated systems and equipment.
Support change controls deviations corrective actions and documentation updates in compliance with site procedures.
Perform routine system checks alarm reviews and basic troubleshooting under the guidance of senior engineers.
Assist with development of URS/FRS documentation and contribute to system upgrades and continuous improvement initiatives.
Ensure all work is compliant with GMP GAMP5 data integrity and site safety requirements.
Collaborate with cross-functional teams including Process Engineering Maintenance IT and Quality.
Requirements
Essential:
Bachelors or Masters degree in Automation Electrical Electronic Mechatronics Chemical or related engineering discipline.
Understanding of GMP manufacturing environments (through internships projects or work experience).
Strong interest in automation technologies (PLC SCADA DCS MES instrumentation).
Good documentation communication and problem-solving skills.
Desirable:
Experience with automation systems or platforms.
Knowledge of GAMP5 CSV data integrity or validation principles.
Previous placement graduate program or internship in pharma/biopharma.
Required Skills:
Essential: Bachelors or Masters degree in Automation Electrical Electronic Mechatronics Chemical or related engineering discipline. Understanding of GMP manufacturing environments (through internships projects or work experience). Strong interest in automation technologies (PLC SCADA DCS MES instrumentation). Good documentation communication and problem-solving skills. Desirable: Experience with automation systems or platforms. Knowledge of GAMP5 CSV data integrity or validation principles. Previous placement graduate program or internship in pharma/biopharma.
We are seeking enthusiastic Graduate or Junior Automation Engineers with exposure to GMP-regulated environments to join our clients high-performing engineering team in Ballydine Co. Tipperary. This is an excellent opportunity for early-career engineers to develop hands-on automation expertise within...
We are seeking enthusiastic Graduate or Junior Automation Engineers with exposure to GMP-regulated environments to join our clients high-performing engineering team in Ballydine Co. Tipperary. This is an excellent opportunity for early-career engineers to develop hands-on automation expertise within a world-class pharmaceutical manufacturing site.
You will work alongside experienced Automation and Process Engineers supporting projects focused on manufacturing systems process controls data integrity and equipment automation within a highly regulated environment.
Key Responsibilities
Support automation activities across manufacturing utilities and laboratory equipment within a GMP environment.
Assist in configuring testing and troubleshooting automation systems (e.g. PLC SCADA DCS systemsAllen Bradley Siemens DeltaV).
Participate in commissioning qualification and validation activities (IQ OQ PQ) for automated systems and equipment.
Support change controls deviations corrective actions and documentation updates in compliance with site procedures.
Perform routine system checks alarm reviews and basic troubleshooting under the guidance of senior engineers.
Assist with development of URS/FRS documentation and contribute to system upgrades and continuous improvement initiatives.
Ensure all work is compliant with GMP GAMP5 data integrity and site safety requirements.
Collaborate with cross-functional teams including Process Engineering Maintenance IT and Quality.
Requirements
Essential:
Bachelors or Masters degree in Automation Electrical Electronic Mechatronics Chemical or related engineering discipline.
Understanding of GMP manufacturing environments (through internships projects or work experience).
Strong interest in automation technologies (PLC SCADA DCS MES instrumentation).
Good documentation communication and problem-solving skills.
Desirable:
Experience with automation systems or platforms.
Knowledge of GAMP5 CSV data integrity or validation principles.
Previous placement graduate program or internship in pharma/biopharma.
Required Skills:
Essential: Bachelors or Masters degree in Automation Electrical Electronic Mechatronics Chemical or related engineering discipline. Understanding of GMP manufacturing environments (through internships projects or work experience). Strong interest in automation technologies (PLC SCADA DCS MES instrumentation). Good documentation communication and problem-solving skills. Desirable: Experience with automation systems or platforms. Knowledge of GAMP5 CSV data integrity or validation principles. Previous placement graduate program or internship in pharma/biopharma.
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