Associate Director Regulatory Affairs

2 weeks ago


Slough, United Kingdom Blackfield Associates Full time

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



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