Senior Regulatory Affairs Lead – Submissions & CMC

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphasis on timely communication and compliance with UK and EU legislation. This is a full-time role offering the chance to work in a dynamic environment with multiple tasks and deadlines. #J-18808-Ljbffr