QA engineer R&D

WHAT ARE YOUR RESPONSIBILITIES?

  • You will provide input from a quality and compliance perspective 
  • You will support the creation of qualification and validation documents in relation with product development projects 
  • You will review project documentation, mainly Design History File
  • You will own the risk management process within the product development project
  • You will ensure issues, deviations and design changes during product development are adequately investigated and documented  
  • You will establish and maintain an adequate quality mindset in the development teams 
  • You will contribute to equipment, method and supplier qualifications

WHO ARE WE LOOKING FOR?

  • You have a master’s degree in life sciences or a PhD (e.g. Biomedical Engineering, industrial pharmacist, bio-engineer, engineering…) 
  • You have experience in a pharmaceutical/GMP environment 
  • You have Knowledge of  ISO 13485, 21 CFR part 820 and ISO14971, ISO62366 as well as knowledge on technical standards, e.g. ISO62304 and GAMP, is an asset
  • You have good communication skills and you are a team player
  • You have good writing skills in Dutch or French and English

WHAT DOES QBD OFFER YOU?

  • A young and dynamic company with a feel good culture, and a great openness and a no-nonsense approach
  • Real investment in people through education and fun events
  • A competence development model focused on your personal ambitions
  • An attractive salary package

Interested? Apply now by sending us your CV and motivation.