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
~ This position is a permeant role, which requires hybrid working 3 days per week in the Slough office. Remote workers not considered.