This role is responsible for executing content management of non-complex local product documents, local label documents, and patient leaflets for nationally registered products. It involves system management for labeling activities, QC of labeling text, and ensuring data integrity. The role requires basic knowledge of labeling and regulatory principles, proficiency in systems, and experience with structured data. Experience in Regulatory Affairs, particularly with product labeling and regulatory guidelines, is important.

This role manages the process of creating and updating labeling artwork for pharmaceutical packaging, ensuring compliance with regulatory requirements and coordinating with various internal and external stakeholders. It involves initiating artwork requests, tracking changes, managing timelines, and ensuring accurate final content for product packaging.