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Validation Engineer / CQV Engineer / 3-5 months project

Plaats: Nederland
Bedrijf: SIRE® Life Sciences

Validation Engineer / CPV Engineer


A big Pharmaceutical client based in the area of Den Bosch / Eindhoven / Nijmegen.

Role Description

We are looking for Validation Engineers for the IT department of this big multinational.


  • Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilisation validation)
  • Field testing Equipment and support commissioning
  • Authoring project validation master plans
  • SOP and documentation updates
  • Authoring validation protocols and final reports, executing validation studies, analysis of validation data
  • Resolving technical issues encountered during study execution.
  • This individual will be required to work in a cross-functional team and independently to accomplish validation project objectives. Minimal work direction needed, highly skilled and knowledgeable to the position.

  • Bachelor or Master in Engineering, Computer Science or other technical degree
  • Equipment Validation and sterilisation Validation experience within a GMP environment
  • Strong technical writing and oral communication skills.

Extra information

Because of the quick start-date of this position we will need a candidate who is currently already living in The Netherlands.



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