QA Validation Specialist

  • Lieu: Mont-Saint-Guibert
  • Type : Perm
  • Travail #13915

QA Validation Specialist

Brabant Wallon – CDI

#validation #QA #masterplanning #qualification #GMP #GDP #GCP

Are you interested in the pharmaceutical industry and putting your knowledge of validation to good use?

Our client is actively looking for a QA Validation Specialist to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As QA Validation Specialist, you are in charge to

  • Put in place an active SVMP and keep it live and up to date
  • Ensure we have a validation system, sops and templates to enable us to perform
  • Meet the ever increasing validation requirements of audits and inspectors
  • Use risk-based approaches to make validation activities efficient, cost-effective and defendable
  • Validation Master Planning
  • Retrospective review of validation activities in order to prioritise and define future work
  • Writing a site validation master plan
  • Be able to lead a validation/qualification
  • Take the lead for validation activities from a Quality Perspective
  • Data Integrity risk assessment and principles

Who are you?

You are graduated as a Pharmacist’s degree or a Master Science. You have 5 years of experience in QA. You have experience in wide range of validation activities-facility qualification, equipment qualification, process validation, cleaning validation/verification. Knowledge of GMP, GDP and GCP is required. You fluently speak French and English.

What can you expect?

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.


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