BrightOwl Loader Loading

Quality Engineer - Consultant for the Biopharmaceutical Industry - Belgium, Switzerland  

Company managed [?] Still accepting applications
46 Facebook  Linkedin

Posted on : 30 March 2017

Project Description


Description:
  • Do you have the potential to be a good consultant?  
  • Are you a team player? 
  • Are you curious? 
  • Do you like a challenge & to solve problems? 
  • Can you think “out-of-the-box”? 
  • Do you have a pragmatic & analytical mindset?  



YOUR RESPONSIBILITIES 
  • You are, in cooperation with a team, responsible for the necessary support and execution of various projects at the client’s site, taking into account timing, expected results and reports, in order to meet the customers’ expectations. 
  • As a Quality Engineer, you may be required to:
    • Support the Quality Assurance team in the verification & release of the products
    • Support the Quality assurance team in different QA processes (change control, deviation & CAPA management, …)
    • Give insights on the Quality Assurance Strategy
    • Verify compliance of production processes with Quality Requirements (GMP, GDP, GLP) & Quality Strategy
    • Define & implement qualification/validation strategies and protocols




WHAT WE CAN OFFER 
  • Our company  is an innovative consulting company, specialized in the bio pharma and company sector.
  • Our company  delivers smart, tailored solutions in the development and optimization of operational quality systems. 
  • Our company  is the market leader in this area and is recognized as innovative, professional and result oriented company.
  • Today, our team counts approximately 70 members.
  •  A dynamic working environment with an open and collegial, yet professional culture
  •  A challenging position in an innovative consulting company
  •  A varied offer of interesting projects and contacts within in the biopharma and company industry
  •  The chance to work with the proprietary company-methods and the chance to participate in the development of innovative solutions
  •  Training and development opportunities at an international level, depending on your experience
  •  An attractive salary package, in accordance with your experience, performance and knowledge 




PROFILE 
  •  You have a master degree in the Life Sciences: Bioscience engineering, engineer, biomedical studies, pharmaceutical studies or related studies
  •  A first experience in the pharma/biotech field of Quality Assurance and control, validation or engineering in a GMP environment is an asset
  •  You feel comfortable to independently solve complex problems by applying pragmatic solutions
  •  You are able to think “out of the box”
  •  You are customer, business and solution oriented
  •  You can work efficiently in multicultural environments
  •  You are fluent in Dutch or French, and you can express yourself in English.