Regulatory Affairs Associate
That's XPE. For one of our clients we are looking for: Regulatory Affairs Associate Organisation description:
Our client, a leading innovative company, active in nuclear medicine, is hiring a motivated, RA associate to strengthen their Belgian team.
ext 2104Job description:
As an Regulatory Affairs Associate, your updated knowledge of the regulations and guidelines and your keen eye for detail will be needed to:
- Compile registration dossiers (DM, DMF, ASMF, …)
- Assist clients in the preparation of their registration dossiers
- Assure international client support
- Be in charge of conformity dossiers
Furthermore, you manage the coordination of the different studies on dossier level.
Finally, you participate in projects related to production (aseptic process, autoclaving,..).Profile:
The ideal candidate has a Scientific Master in for example chemistry, pharmacy, biomedical sciences, biology,… and you have a relevant first experience in the pharmaceutical industry and/or in Regulatory Affairs.
English and French hold no secrets from you and you can effectively and fluently communicate both in writing and orally.
And finally, if the words: persistent, curious and pro-active; cover your personality, you are the Regulatory Affairs Associate I am looking for!Offer:
You are offered a permanent, full time contract directly on our client's payroll.
You gain experience in an innovative, flexible and dynamic working environment and get the chance to contribute to the improvement of cancer diagnosis and therapy techniques!
XPE Personnel Services NV/SA: Flanders: VG15/BU, Brussels: B-AA5.031, Wallonia: W.RS.002/W.INT.002 XPE Group NV/SA : Flanders: VG1834/B, Brussels: B-AA11.007, Wallonia: W.RS.713