Description
This role involves leading process management for regulatory submission documents, ensuring timely and high-quality submissions aligned with pharmaceutical affairs regulations. Responsibilities include eliminating bottlenecks, proposing efficient processes, evaluating and optimizing internal systems, and acting independently as a SubM & RC. The role contributes to problem resolution, develops junior employees, manages dossier structures, drafts timelines, leads intermediate reviews, tracks progress, mitigates risks, and ensures compliance with regulatory requirements.
