Senior Automation Engineer – DeltaV Expert in GMP Systems

UNAVAILABLE

Cork

On-site

EUR 70,000 - 100,000

Full time

14 days+

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Job summary

Hovione in Ireland Cork is seeking a Senior Automation Engineer to join our Automation team. This senior individual contributor role provides technical leadership across design, lifecycle management, validation, troubleshooting, and continuous improvement in a GMP manufacturing environment.

You will design and implement DeltaV-based automation solutions, support system upgrades, and ensure compliance with GMP, 21 CFR Part 11, and internal quality standards.

Qualifications

  • Degree in Automation Engineering or related discipline.
  • Minimum 5 years in industrial automation.
  • Strong DeltaV programming and configuration experience.
  • Experience with GMP and 21 CFR Part 11.
  • Excellent problem-solving and root cause analysis skills.
  • Fluent English, written and spoken.

Responsibilities

  • Maintain and optimize automation systems and process control.
  • Design, develop, configure, and implement DeltaV solutions.
  • Troubleshoot and resolve complex automation issues in live production.
  • Provide technical guidance to manufacturing, engineering and process teams.
  • Develop and maintain standards for alarms, interlocks, and HMIs.
  • Support commissioning, qualification, validation activities and lifecycle management.

Skills

DeltaV programming
System troubleshooting
Regulatory compliance
GMP knowledge
Project management
Stakeholder mgmt

Education

Degree in Automation Engineering
Bachelor's in Chemical Engineering

Tools

Emerson DeltaV

Job description

Hovione in Ireland Cork is seeking a Senior Automation Engineer to join our Automation team. This senior individual contributor role provides technical leadership across design, lifecycle management, validation, troubleshooting, and continuous improvement in a GMP manufacturing environment.

You will design and implement DeltaV-based automation solutions, support system upgrades, and ensure compliance with GMP, 21 CFR Part 11, and internal quality standards.

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