Description
For our client, a global player in the life science industry with more than 80 000 employees globally we are currently looking for a Regulatory Affairs Expert who- has more than 5 years experience in CMC (Module 3), technical writing
- small molecules and drug products experience
- eCTD extendo and/or gunter knowledge preferred
- packaging, approving of art work
- experience in global submissions of dossiers
- life cycle management of products
- hands on writing and designing of dossiers to various agencies globally
- English
- candidates have to have a valid work permit for Switzerland
This position is limited to 6 months with a possibility of extension. You have to be available 5 days a week at client's location.
If you fulfil the requests feel free to forward your application to Lukasz Zawadzki or call me under .
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>