Role Overview
This is an exciting opportunity for an experienced regulatory professional to shape the global CMC regulatory strategy for an innovative portfolio of mRNA medicines. Working across multiple development programs, you will play a critical role in driving international regulatory submissions, influencing product development, and ensuring the highest standards of regulatory compliance.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.