Senior Regulatory Affairs Officer - West London

Key People Limited
London (Greater)
12 Jan 2018
11 Feb 2018
Contract Type
Full Time
An excellent opportunity has arisen for a Senior Regulatory Officer to join a Pharmaceutical company based in West London - hands on eCTD submission experience is essential.

Within this role you will be responsible for registering an exciting range of new products and maintaining a European Portfolio. Working in a small team, you will be exposed a vast range of responsibilities and gain a huge amount of experience within a short amount of time!

Responsibilities include:
- Ensure regulatory submission (DCP's, MRP's and National applications) are completed in a timely manner using eCTD
- Perform routine regulatory activities (i.e. maintenance/renewals, variations, 61(3) notifications)
- Aid in technical input where required
- Ensure artworks are created and approved in time for product launches
- Maintain current knowledge of regulatory affairs legislation
- Ensure all regulatory databases are kept up to date
- Provide support for marketing material

Experience required:
- Hands on eCTD submission experience is essential
- 2-4 years of regulatory experience
- Ideally a generics background