Associate Director Regulatory Affairs

Our client, a global pharma company that's innovating in the Neurology and Injectables market, has a requirement for an Associate Director Regulatory Affairs to join their Slough based European HQ.

To be considered for the role of Associate Director Regulatory Affairs, you will have experience in: 10 years plus regulatory experience, ideally gained in a generics or R&D business Lead PIP submissions to EMA authorities CTIS submissions to EMA bodies Previous experience with a Neurology and injectables portfolio, including due diligence Respiratory experience would be desirable This position is a permeant role, which requires hybrid working 3 days per week in the Slough office.
Remote workers not considered.

Must hold valid right to work- Unable to sponsor