NonStop Recruitment
This job has been posted for more than 30 working days and has expired.

Regulatory Affairs Project - IVD - Belgium

A global pharmaceutical company is looking for a Regulatory Affairs Project Manager who will work on a new 1 year project with a global scope.

The Regulatory Affairs will be for in vitro diagnostic products which is a more niche area where you can use your expertise and gain even more experience.

IVD products are very important and more complex.

Therefore your work will be very appreciated in the global healthcare industry.


  • Bachelor or Master in Life Sciences

  • More than 5 years of working experience in Regulatory Affairs

  • Experience with IVD Directives in EU, knowledge of US Directives are an advantage

  • Project Management skills

  • Fluency in English required, Dutch or French plus

The company has a lot of products on the global market and has built out a good reputation.

Next to that they still invest a lot in Research and Development.

Accordingly your can add this experience on your CV and secure good future opportunities.

The company is big and works with a lot of contractors so it will give you more chance on other contracts in the company.

If this job appeals to you please send me, Annelies De Baere, your most recent CV in Word format to or call me on +32 2 403 49 80.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe.

We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry.

Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences for all EU8 countries.

Please visit our website for a full list of the niche markets we cover.