At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Responsibilities include supporting the preparation of regulatory submissions (e.g., NDA, BLA, and post-approval changes) as well as manufacturing technology transfer to commercial sites. The role also drives the exploration and evaluation of new technologies within FTRL and serves as an integral contributor to decision-making processes in the Formulation Technology Research Laboratories * Lead manufacturing technology transfer activities, primarily to Daiichi Sankyo Europe and CDMOs in the EU, as well as pivotal formulation development.
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