Description
The Regulatory Labeling Manager supports the planning, coordination, and execution of EU and global labelling compliance activities across the Regulatory Affairs organisation. The role manages labelling change requests, Product Information updates, linguistic reviews, artwork approvals, implementation workflows, vendor coordination, inspection readiness, process improvement, and stakeholder communication. It requires a bachelor’s or master’s degree and 9 to 12 years of directly related experience in regulatory affairs, labelling compliance, artwork management, quality, or a related pharmaceutical or biotechnology function.
