Description Overview
As a member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Associate will focus on post marketing regulatory activities for medicinal products within UK and Ireland.
This role is a 6-month Fixed Term Contract.
Scope of the Role
Work on Regulatory Affairs projects & product changes to meet business needs.Comply with the existing legislation and regulations for medicines.Ensure product registrations are correct and compliant with the relevant legislation.Establish, review, approve and update regulatory documentation.Prepare & submit variations via the electronic platforms.Maintain accurate and complete records by updating the relevant trackers, product folders and regulatory databases.Approve Artwork and Texts from a regulatory perspective.Participate in project meetings with both internal a...