Pauwels Consulting
EN
CSV
Pharma & Sciences - Validation - wavre
  • 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
Reference number: 48193

What are we looking for?

  • 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 

What do we offer?

  • 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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