Regulatory Affairs Director, MDR and Biologicals, Belgium
For an innovative Pharmaceutical Company based in Flanders, Belgium; I am looking for a Regulatory Affairs Director who will be responsible for the global registrations of medical devices and biologics.
In this role you will manage a small RA team and in addition you be the main contact for Regulatory authorities with regard to product information and issues.
- You have a Master or PHD in a life science discipline
- Minimum of 6 years working experience in Regulatory Affairs in the Pharmaceutical industry
- Excellent knowledge of the latest MDR/ EU requirements, GMP, ICH, GMP and GDP
- Experence in people management and you are able to develop and motivate your team
This is career defining role for the right person.
If you are interested; sent me your contact details and I will contact you within 24 hours or you can also sent me an email at: email@example.com.
Or if you know of someone who could be interested; share this vacancy and help the people in your network.