You will be responsible for developing and managing the licensing process for submissions within the UK and International markets.
You will work with a small team of Regulatory Affairs professionals who enable our organisation to deliver against its growing licensing business opportunities.
Main duties of the job:
You will be a clear leader, motivated and highly organised, achieving a high standard of work to agreed deadlines.
Reporting to the Head of Regulatory Affairs, you will enjoy working autonomously in all aspects of from initial regulatory assessment of a potential licensed product through to supporting commercialisation. It is essential that you have a clear understanding of the technical challenges within pharmaceutical manufacturing to facilitate a successful project.
Regulatory Affairs is multi-disciplinary and therefore this role will require much personal interaction and excellent communication
To speak to a recruitment expert please contact Alba Subinas