Director, Regulatory Site CMC

As a Director of Regulatory Site CMC at Takeda, you will lead site-specific post-approval change management for small molecules and biologics, ensuring compliance with global regulatory requirements beyond the EU and US. You will apply science- and risk-based approaches guided by ICH Q12 principles to streamline processes, drive automation, and support diverse manufacturing sites and external partners. This role requires communicating regulatory strategy to cross-functional teams and fostering scalable, sustainable operations across global operations.