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 in Ireland and manage their Global Submissions.
Reporting into the Head of Regulatory Affairs, the successful candidate will be responsible for managing Global Submissions.
In order to be considered you must have the following:
- A PhD, MSc or BSc
- A minimum of 5 years of Pharmaceutical Regulatory Affairs experience
- Hands on experience of managing Global Submissions for both marketed and products under development
- 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.