Regulatory Affairs Associate (CMC Lifecycle)

This role offers the opportunity to develop strong regulatory expertise in post-approval CMC changes across EU and international markets, while gaining exposure to cross-functional collaboration with Manufacturing, MS&T, Quality, Supply Chain, Submission RA and external partners/CMOs. On this role you will work in a dynamic, multinational environment with broad stakeholder interaction and visibility, and will have the chance to contribute to process improvement, standardization and more efficient ways of working within RA CMC Lifecycle.