Automation Engineer - Delta V

EFOR; Limerick; Hybrid; EUR 65,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Career development opportunities

Job summary

EFOR is seeking an Automation Engineer to deliver automation solutions for pharmaceutical manufacturing projects. The role spans design through commissioning, qualification, and operational support.

You will design DeltaV DCS configurations, support FAT/SAT, and collaborate with validation teams to ensure GMP compliance. The position offers hybrid work arrangements across multiple locations and a competitive salary with benefits.

Qualifications

• Experience as an Automation Engineer in pharmaceutical or life sciences industries.
• Strong hands-on DeltaV experience.
• Knowledge of GMP-regulated manufacturing environments.
• Experience with commissioning, qualification, and validation activities is desirable.

Responsibilities

• Design, develop, configure, and troubleshoot DeltaV DCS systems.
• Support FAT, SAT, commissioning, and start-up activities.
• Develop and modify control strategies, graphics, and batch recipes.
• Collaborate with multidisciplinary engineering and validation teams.
• Ensure GMP, GAMP 5 and industry standards compliance.
• Provide ongoing technical support for manufacturing operations and capital projects.

Skills

Problem solving

Communication

On-site/Hybrid collaboration

Tools

DeltaV

Job description

We're looking for experienced Automation Engineers to support leading pharmaceutical manufacturing projects across multiple locations. If you have a strong background in process automation and hands-on DeltaV experience, we'd love to hear from you.

About the Role

As an Automation Engineer, you'll be responsible for delivering automation solutions for pharmaceutical manufacturing facilities, supporting projects from design through commissioning, qualification, and operational support.

Key Responsibilities

• Design, develop, configure, and troubleshoot DeltaV DCS systems.
• Support FAT, SAT, commissioning, and start-up activities.
• Develop and modify control strategies, graphics, and batch recipes.
• Collaborate with multidisciplinary engineering and validation teams.
• Ensure compliance with GMP, GAMP 5, and pharmaceutical industry standards.
• Provide ongoing technical support for manufacturing operations and capital projects.

Requirements

• Experience as an Automation Engineer within the pharmaceutical or life sciences industry.
• Strong hands-on experience with DeltaV.
• Knowledge of GMP-regulated manufacturing environments.
• Experience with commissioning, qualification, and validation activities is desirable.
• Excellent problem-solving and communication skills.
• Ability to work on-site or in a hybrid environment, depending on project requirements.

Locations

We have opportunities across multiple locations, with roles available on a variety of exciting pharmaceutical projects.

Why Join Us?

• Work on cutting-edge pharmaceutical manufacturing projects.
• Competitive salary and benefits.
• Career progression and continuous professional development.
• Collaborative and supportive engineering environment.