Our client is a biopharmaceutical company focused on developing and delivering innovative new treatments to help improve the lives of patients with rare and orphan diseases. They have a growing commercial business and a significant development pipeline. They have a new opportunity for an experienced Regulatory Affairs Professional to join the Regulatory Department based out of Dublin.
Reporting into the Head of Regulatory Affairs, the successful candidate will act as subject matter expert for publishing and submissions activities for global markets.
In order to be considered you must have the following:
- A PhD, MSc or BSc
- A minimum of 5 years Pharmaceutical Regulatory Affairs experience
- Experience generating global publishing strategies and an ability to develop and maintain submission content plans - for both EU and US markets
- Eligible to live and work in the EU
To discover more about this opportunity, apply now or contact Gillian McMurrough at HRM on +353 871213548 for a confidential discussion.