Regulatory Affairs Associate

**The Regulatory Affairs Associate is responsible for assisting the Regulatory Affairs team in our Italian affiliate.
Sound interesting?
Then read on**
Ultimately, at Norgine, we look for the following skills and experience in our Regulatory Affairs Associate;
- Some experience in the pharmaceutical industry
- An awareness of the drug development process
- Developing regulatory knowledge for medicinal products and medical devices
- Developing product knowledge
- Ability to pragmatically interpret GxP and Code of Practice or internal processes requirements relevant to her responsibilities
- Training in Applicable Codes and keep up to date with applicable case law (Knowledge and skills should be maintained by appropriate updates and training)
- Demonstrates a good ability to analyse data
- Focused on customer needs, follows up on commitments and requests
- Good interpersonal skills
- Good verbal and written communication skills
- Works cooperatively within a team
- Good ability with Microsoft Office (Word, Excel, PowerPoint)
- Ability to communicate clearly in English
**Norgine has a direct presence in 16 European countries, as well as Australia and New Zealand.
We also have a strong global network of partnerships in non-Norgine markets.
We are a flexible and fully integrated pharmaceutical business, with manufacturing (Hengoed, Wales and Dreux, France), third party supply networks and significant product development capabilities, in addition to our sales and marketing infrastructure.
This enables us to acquire, develop and commercialise specialist and innovative products that make a real difference to the lives of patients around the world.