Job Description
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