Description
Are you a chemist with 5 years experience with global Regulatory Affairs technical submission strategy experience? Than keep reading.My client - a global Pharma company with over 8000 people from approximately 80 countries located in Basel region is currently looking to assist their team with an expert who can:
- provide strategic leadership and regulatory decision for synthetic marketed products
- develop global CMC regulatory strategy
- manage high quality regulatory submissions (changes, renewals CTA) globally
-interact with management from different internal functional areas
we expect from you:
- a strong science or technical background (RA)
- Master or PhD in chemistry, pharmacy or relevant engineering
- 3 to 5 years experience in drug development of small molecules
- NDAs and/or post-approval submissions
- demonstrated leadership, strong prioritization
- fluent in English and German is an advantage
If you fulfil the minimum criteria and are interested in this position or similar ones, contact me today, for immediate consideration.
Lukasz Zawadzki
Email:
Tel:
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>