Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input
Overview In this role you drive analytical development for gene editing and nucleic acid-based therapeutics within the GRD CMC team. You lead method development and control strategies for complex modalities, including ATMPs and LNP-based products, collaborating across
Overview As Global NPP Manager, you drive early pipeline assessment and inorganic growth initiatives for the AIR Franchise. You analyze market landscapes, competitive dynamics, and revenue potential to shape investment stories and commercial strategies. You work