Pauwels Consulting


Pharma & Sciences - Validation
  • Provides technical expertise and supports all Validation aspects in the project
  • Reviews and approves the Qualification and Validation protocols and reports to ensure compliance with the current regulations
  • Supports Data integrity and risk assessments
  • Creates and maintains the validation documentation and other relevant GxP documents within the Document Management System
  • Manages and executes Periodic Reviews
Numéro de référence (48193)

Que recherchons-nous ?

  • Bachelor or Master’s degree in pharmaceutical sciences field (biology, chemistry, chemical,…) or relatable experience. 
  • Proven experience in Computerized System Validation is a MUST
  • 1-5 years’ experience in Quality Assurance, in a regulated environment (pharma, biotech) 
  • Good knowledge of GMP, deviation, CAPA, Changes control, Risk Management and quality systems 
  • Autonomous, conscientious and positive problem-solving mindset. 
  • Fluent in French and good level of English 

Que proposons-nous ?

  • 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

Dans quelle ville travaillerez-vous ?

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Nous acceptons les documents Office et les fichiers PDF. Les documents doivent avoir une taille maximale de 10 mégaoctets.
En bref
employé, travailleur indépendant
40 par semaine
Jahlye Geeraerts
Jahlye Geeraerts
Talent Acquisition Specialist Life Sciences