Validation Engineer

A pharmaceutical OSD Manufacturing site based in Wicklow have a permanent opening for a Validation Engineer to join their QA Team.

Reporting directly to the Validation Supervisor, this is a role that is hands-on as you will work between the QA and production teams.

You will have the opportunity to work in lab equipment validation, process validation and cleaning validation.

This would be a great opportunity to gain experience in all areas of Validation, and to work on a small team with lots of responsibility.

As Validation Engineer, you will be responsible for;

  • Co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation in the Production Department
  • Preparation and execution of validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of equipment, systems, products and projects
  • Process Validation regulatory requests relating to the VMP
  • Acting as the primary point of contact for all Production related Validation matters as well as internal and external compliance audits or regulatory inspections

Education and Experience;

Degree qualification in a Scientific Discipline

At least 2 years' experience in Validation within the pharmaceutical or medical device industry

Excellent Salary and Benefits package on offer with this role.

Not sure yet? No CV Ready? Give me a call on 01-8883477 for more information!

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