Experienced Regulatory Affairs Professional EMEA

Job Description
EMEA Regulatory Affairs Solid Tumours is recruiting for a dedicated Experienced Regulatory Affairs Professional to work on the development and registration of solid tumour products in Europe, the Middle East, and Africa (EMEA). The Regulatory Affairs Professional supports the development, registration, and lifecycle management of pharmaceutical products within the EMEA region. This role focuses on regulatory tasks such as submission strategies, procedural aspects of regulatory affairs, and compliance with applicable health authority (HA) regulations, project management, and would support the EMEA regulatory leader on regulatory product strategy. The position can be based in Belgium, The Netherlands, Poland or the United Kingdom. This is a hybrid role, meaning regular office presence is required in coordination with your team. This role provides an opportunity to support small and large molecules, and in different oncology indications, contributing to advanceme...