EU Regulatory Affairs Lead - Medicines & Devices

A public health regulatory agency in Greater London seeks a Principal Policy Lead to oversee EU regulatory initiatives in medicines and medical devices. The successful candidate will manage stakeholder engagement, coordinate cross-MHRA projects, and draft policy recommendations for government leaders. This full-time, permanent role offers a hybrid work environment requiring at least 8 on-site days per month. An ideal candidate will have experience in public sector engagements and understanding of health and life sciences.