Join our UK Regulatory team and play a central role in delivering strategically important, timely and high quality submissions that help bring innovative medicines and devices to patients.

Your new role

As Regulatory Affairs Lead you will manage, plan and execute regulatory projects within the UK Regulatory, Safety & Medical Information (RSM) team. You will provide technical and strategic support to the Associate Director of RSM and to UK Regulatory Affairs (UKRA), partner with business units to align regulatory files and labels with business and patient needs, and lead complex MAA submissions and lifecycle changes (including new products, line extensions and strategic projects) with the MHRA.

Day to day your tasks will include:

• Lead regulatory projects end to end: planning resources and budgets, developing and leading the regulatory strategy, performing risk analysis and delivering implementation plans.
• Act as UK point of contact...