Regulatory Affairs Associate
Berkshire (UK) – Hybrid
Regulatory Affairs Associate opportunity working for a multinational pharmaceutical company that works across tuberculosis, diabetes, cardio, respiratory, women’s Health and the central nervous system (CNS).
As a Regulatory Associate, you will be responsible for managing regulatory submissions and variations applications for a range of different generic products.
Responsibilities
- Take responsibility for post- approval activities including, variations (type 1a, 1b, and type 2), renewals, and license changes.
- Preparation, submission and management of variation applications to agreed timelines.
- Preparation, submission and management of approvals of National, Mutual Recognition and Decentralised Procedure applications in the UK and European region.
Requirements
- Bachelor’s degree or higher in Life Sciences or technical field.
- 18 months to 2 years of relevant regulatory experience.
- Previous EU market experience with strong experience submitting through decentralised procedure
This position allows for great career progression opportunities as well as the chance to work for a multinational organisation. The role includes some excellent benefits such as a 6-12% bonus, private health insurance, pension scheme, life insurance, 28 days holiday, and a range of other benefits.
If you are interested in this role or would like more details please email your CV to lucy.kirkaldy@cpl.com
- Agency: Cpl Life Sciences
- Reference: JO-2212-507005
Website: Cpl Life Sciences
- Posted: 3rd March 2023
- Expires: 31st March 2023
