Who are we? We are eyetec!
eyetec is a European reference player in providing services and machinery in the pharmaceutical sector (production, research, and hospitals). 

One of our core activities is supporting clients in the introduction and startup of pharmaceutical equipment according to the applicable norms and standards.

You will join a small but growing team of curious, independent, and flexible employees who plan their day and work based on trust. Add a dose of fun, and you have an idea of where you will end up! Does this sound like music to your ears? Then read on!

What will you do as a Qualification Engineer lead?
As a Qualification Engineer, you will be responsible for the delivery, qualification, and validation activities during the introduction of pharmaceutical equipment.

Let's get concrete now!
You support the introduction of new or existing installations.

  • You take the technical lead in the installation of new pharmaceutical installations or the  optimization of existing machines.
  • You guide the delivery, qualification, and validation activities.
  • You create or screen the user requirements.
  • You conduct technical reviews of designs and design documents.

But you are also a star as a project leader within a GMP context:

  • You closely monitor your projects from A to Z.
  • You collaborate with the client's technical, quality, and engineering services.
  • You manage the scope, timing, and budget of your project.
  • You communicate accurately and efficiently to all your stakeholders.
  • You ensure reporting and documentation in line with the applicable standards.
  • You constantly develop your knowledge of technical evolutions in the pharmaceutical industry and GMP standards.

As a Qualification Engineer, we would like to see the following knowledge and experience in you:

  • You have a professional Bachelor's or Master's degree in Engineering in Electronics, Electromechanics, Chemistry,  Automation, or equivalent through experience. Do you have a different degree and still think you qualify for this position? Convince us by thoroughly motivating your choice.
  • Ideally, you have several years of experience in Qualification Engineering in a GMP context. If not, we will take the necessary steps together to bring your knowledge up to level with relevant training.
  • You have an analytical mind and unravel problems to come to the most suitable technical solutions.
  • Technology is your 'thing,' and you want to push eyetec further forward in your field.
  • You are a team player who fits within the ambitious and informal atmosphere of eyetec.
  • You can work independently and punctually but also function smoothly in a team, both at the client and within the eyetec team.
  • You are communicatively strong and can express yourself fluently in Dutch and English. Knowledge of French is a plus.
  • Your technical writing skills are excellent.
  • You work about 15% to 20% of your time abroad (Europe).

Nodding in agreement while reading all this? Then we have a lot to offer!

  • You will receive intensive training in an exciting and complex market.
  • You will get the necessary tools to do your job, such as a company car, mobile phone, and laptop.
  • You have the opportunity to grow in a young and driven company with a family atmosphere and no-nonsense communication.
  • We offer you a challenging full-time job, an attractive salary, and attractive extra-legal benefits (group insurance, meal vouchers, net bonus premium, etc.).
  • The place of employment is eyetec, Kemelbeekstraat 80D, 2460 Tielen. Possibility of working from home. Our clients are typically in Belgium, with some international clients in Switzerland, Germany, and Austria.

Are you intrigued by eyetec and feel attracted to this unique role? Are you determined to support this growth trajectory, with attention to our clients, quality, and your team? Then do not hesitate to click and apply below. 

apply now