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 monthly wage, car, fuel card, (super fast) bicycle, insurance package, meal vouchers, etc.

But most of all..

  • Working for the Antwerp Young Entrepreneur of 2019!
  • A flat organization in the broadest sense of the word
  • An increase in your IQ through our extensive training package
  • A hip office with air hockey table
  • More muscle mass through our weekly boot camps
  • 32 vacation days that you wish were fewer (because it's great to work here 😉 )
  • In short … We work, we play, we deliver, we are Quality by Design!

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