DELTAV AUTOMATION ENGINEER (482)

Réalta Technologies

Dublin

On-site

EUR 65,000 - 90,000

Full time

11 days ago
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Job summary

Réalta Technologies, based in North Dublin, seeks an experienced DeltaV Automation Engineer for a leading pharmaceutical client. 5+ years in automation within pharma/life sciences and hands-on DeltaV across the project lifecycle are required.

The role involves design, configuration, testing, validation, and site commissioning in a GMP environment.

Qualifications

  • : 5+ years in Automation / Controls Engineering.
  • :

Responsibilities

  • Provide automation engineering support throughout the full project lifecycle, from design through to commissioning and start-up.
  • Develop and configure Emerson DeltaV DCS systems in line with project requirements.
  • Develop and review automation documentation, including functional specifications and design documentation.
  • Support and execute FAT, SAT, testing and commissioning activities.
  • Troubleshoot and resolve DeltaV and automation system issues during testing, commissioning and start-up.
  • Support the successful handover of automation systems to site operations.
  • Work within relevant GMP and pharmaceutical engineering standards.

Skills

Automation / Controls Engineering
DeltaV DCS
GMP experience
Life sciences
Project lifecycle

Education

Engineering qualification in Automation/Controls

Tools

Emerson DeltaV

Job description

Réalta Technologies are seeking an experienced DeltaV Automation Engineer to join a leading pharmaceutical client based in North Dublin.

The successful candidate will have 5+ years' experience in automation engineering within the pharmaceutical or life sciences industry, with strong hands-on experience working with Emerson DeltaV across the full project lifecycle.

Job Responsibilities
  • Provide automation engineering support throughout the full project lifecycle, from design through to commissioning and start-up.
  • Develop and configure Emerson DeltaV DCS systems in line with project requirements.
  • Develop and review automation documentation, including functional specifications and design documentation.
  • Support and execute FAT, SAT, testing and commissioning activities.
  • Troubleshoot and resolve DeltaV and automation system issues during testing, commissioning and start-up.
  • Support the successful handover of automation systems to site operations.
  • Work within relevant GMP and pharmaceutical engineering standards.
Job Requirements
  • 5+ years' experience in Automation / Controls Engineering.
  • Proven experience working with Emerson DeltaV DCS.
  • Pharmaceutical, biotechnology or life sciences industry experience.
  • Experience across the full project lifecycle, including: Design, DeltaV configuration, Testing / FAT / SAT, Commissioning and Start-up.
  • Experience working in a GMP-regulated environment.
  • Relevant engineering qualification in Automation, Electrical, Electronic, Instrumentation, Controls Engineering or a related discipline.
Desirable
  • DeltaV Batch experience.
  • Experience with pharmaceutical validation / CSV activities.
  • Experience with PLC, SCADA or MES systems.
  • Experience on greenfield or brownfield pharmaceutical projects.
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