BioNTech

The manager will establish and improve a global quality assurance framework to ensure GMP compliance for MAH and Sponsor activities. They will also lead the end-to-end lifecycle of product quality complaints, ensuring effective investigation, reporting, and cross-functional collaboration.

Lead global labeling activities for the development and maintenance of Company Core Data Sheets, US prescribing, and EU patient information for commercial products. Define and execute labeling strategies for life cycle management while leading cross-functional teams and regulatory processes.