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Validation Antwerp Belgium, Breda Netherlands,  

QBD (company)


Posted on : 04 April 2017

Project Description


What are your responsibilities?
  • As a Validation or Qualification engineer you are responsible for the implementation of new systems or changes to existing systems in a controlled and documented way
  • The fields of expertise in which you will work range between production and IT, between QA and SQA, depending on your own interests and ambitions 



Requirements:
  • Master degree with scientific background: (industrial) pharmacist, bio-engineer, industrial engineer, biomedicine or relevant experience
  • At least 3 years of relevant experience in the pharmaceutical industry
  • Quality is a high standard to you since it is a crucial value in the pharmaceutical and biotech industry
  • You are able to manage small, medium or large project depending on your level of expertise
  • You have very good communicative skills
  • Prince2, PMBOK or SixSigma certifications are a plus
  • Knowledge of BPM (Business Process Management) is a plus
  • You have a strong customer focus and service-oriented attitude
  • You can take the initiative and come up with new ideas
  • You are flexible and able to deal with stress 



Offer:
  • A young and dynamic company with a feel good culture, an 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 

Locations

Wilrijk BelgiumBreda Netherlands

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