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Process Validation Engineer

Pauwels Consulting | Liège | Permanent, Independent, Full-time

Published on 12 days ago

Process Validation Engineer

Job description

  • Define the (continuous) validation strategy based upon the guideline and benchmarks for a specific value stream
  • Manage the validation master plan for the value stream 
  • Communicate with the production team to have raw material/assemblies/resources for the validation
  • Write the validation protocols
  • Train operators in SOP, work instructions and protocols, related to the validation
  • Follow up the validation runs on the production floor perform the sampling or IPC testing as required
  • Follow up the QC results for each run of validation
  • Write the validation report
  • Manage, write, investigate and follow up of all deviations related to the validation study
  • Gain experience of the subject to become the validation expert, by working together closely with the production team
  • Act as an SME during inspections/audits


  • Master’s degree or bachelor’s degree in a technical discipline : chemistry, physics, engineering, biochemistry
  • Minimum 3-5 years of operational experience in a pharmaceutical environment
  • Shows good understanding of GMP repository, with ability to translate to operational details
  • Excellent knowledge of French and good knowledge of English (spoken, written, read)


  • Challenging projects based on your interests and skills
  • Personal follow-up and clear, transparent communication both before and after commencement of employment
  • Possibility to follow extra training
  • Inspiring network events and legendary after work drinks
  • Strong network of industry leading clients
  • Expertise within IT, Engineering and Life Sciences
  • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees


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  • Master (University or Higher Education Long Type)


  • Permanent
  • Independent
  • Full-time
  • Company car

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