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・The Associate Director, IMP Quality Advanced Therapies is responsible for developing and executing quality strategies which ensure advanced therapy (e.g. cell and gene therapy) Investigational Medicinal Product (IMP) utilized in Takeda clinical studies is produced in compliance with applicable regulations and Takeda quality expectations, and is released in a timely manner to meet clinical study and developmental timelines.
・This position directly manages the development, implementation, and maintenance of GMP quality operations which support pharmaceutical development and the IMP supply chain (manufacturing, packaging, testing, and distribution) for advanced therapy programs.
・The Associate Director, IMP Quality Advanced Therapies ensures execution of continuous improvement through idea development, plan creation, implementation, and championing project management methodology for projects of high complexity and risk.





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