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    Validation Engineer - Quality Systems

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Validation Engineer - Quality Systems

The Company
The company is a Belgian Biopharmaceutical company, specialized in the production of intermediates and finished products out of blood plasm. They are currently expanding their business and therefore we are looking for a Validation Engineer. 

Role Description
The Validation Engineer will be responsible for everything regarding Validation within the plant. He/she will conduct Method Validation, Process Validation, Equipment Validation and CSV. Furthermore, the Validation Engineer will coordinate a team of consultants on site.


  • Conduct validations within production and QC labs
  • Writing and review of qualification/validation documents
  • Participate in improvement projects regarding validation
  • Maintain the GMP standards
  • Handling of CAPA's, risk assesments, change controls and deviations
  • Give training to other personnel regarding validation
  • Coordinate consultants on site during projects


  • BSc. / MSc. Pharmacy in Life Sciences / Engineering
  • 3+ years of experience in validation
  • Extensive knowledge of GxP
  • Fluent in Dutch/English or French/English
  • Strong communication skills 
  • Experience with Trackwise is seen as an asset

Other information
My client is offering an undetermined contract with a good basic salary, topped up with attractive extra benefits (39 Holidays, Pension Plan, possibility for Company Car, Health Insurance, ...)