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Validation Engineer - West of Ireland


Validation Engineer required for a new Pharmaceutical capital project in the West of Ireland.

Engineer Manufacturing
Years of Experience Req.:
3 years+
Date Posted:
Days Remaining:
Employment Type:
Education Level Req.:
Third Level Degree

Validation Engineer

DPS currently have a requirement for a Validation Engineer with a Pharmaceutical organisation based in the West of Ireland. 


  • As a Validation Engineer you will be responsible for all relevant Process / Equipment Validation activities.
  • Generation and execution of equipment validation lifecycle documentation
  • Review of vendor prepared/executed commissioning & validation documentation
  • Reporting of Validation non-conformances and providing solutions to remediate issues
  • Working with cross function departments to ensure solutions are implemented in an efficient and effective manner
  • Review of the impact of change on the maintenance of the validated state, including execution of re-validation as required
  • Processing documentation through the document management system
  • Periodic review of documentation management system workflows to ensure both regulatory & business needs are satisfied


  • Third Level Degree in Engineering or Science
  • Must have previous work experience within a Pharmaceutical or Medical Device environment.
  • Should have a track record of carrying out and executing GMP/FDA documentation.
  • Innovation/ problem solving abilities, someone who will look through the whole process chain to identify and solve a problem, as well as identify improvements

 To discuss this opportunity further contact Andrew Curtin on 01 466 1797



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