Gra Cmc Director - Marketed Products Development Lead
takeda
Zurich, Switzerland
Hybrid
10+ years pharmaceutical regulatory cmc experience
Expert in developing alternate strategies
Experience with active pharmaceutical ingredients
The Director of Global Regulatory Affairs CMC Marketed Products Development at Takeda in Zurich is responsible for developing and executing regulatory strategies for lifecycle management of marketed products. The role requires extensive experience in regulatory affairs, leadership capabilities, and the ability to navigate complex regulatory environments
Job Summary
Join Takeda as Director, Global Regulatory Affairs CMC Marketed Products Development Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management.
You will lead a team and ensure their effectiveness in a complex matrix environment.
Stay up to date with current and evolving regulatory CMC requirements and apply this knowledge to assigned projects.
Matching Summary
Match Score: 85
The Director of Global Regulatory Affairs CMC Marketed Products Development at Takeda in Zurich is responsible for developing and executing regulatory strategies for lifecycle management of marketed products. The role requires extensive experience in regulatory affairs, leadership capabilities, and the ability to navigate complex regulatory environments.
Skills & Requirements
Must-have
10+ years pharmaceutical Regulatory CMC experience
Expert in developing alternate strategies
Experience with active pharmaceutical ingredients
Nice-to-have
International experience preferred
Ability to influence at all levels
Demonstrate leadership and problem-solving ability
Key Requirements
BS/BA Degree in a Scientific Discipline
Advanced Degree preferred
Understanding of scientific principles and regulatory CMC requirements