Introduction

Our client is a long-established organisation in the specialist pharmaceuticals sector, supplying essential injectable medicines used across critical care settings. They operate within an international group with a strong reputation for product quality, patient safety and collaborative working. The team you would be joining is known for its supportive environment, cross-functional cooperation and commitment to continuous improvement, offering an excellent culture for individuals who enjoy both structure and autonomy.

This role will offer you

The chance to work in a globally connected Medical Affairs function with exposure to international partners and regulatory authorities. A meaningful role where your work directly supports patient safety and compliance across a broad portfolio of critical medicines. Professional growth through involvement in advanced PV activities such as signal management, aggregate reporting and risk management. An opportunity to influence best practice through process improvement, SOP development and collaboration with senior leaders including the QPPV.

You will be responsible for

Managing the end-to-end handling of global safety data, from initial receipt through to assessment and regulatory re...