The role is responsible for formulation design and process development across various modalities, with a focus on ADCs, within the Formulation Technology Research Laboratories (FTRL). 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 * In-depth knowledge of global CMC development, particularly formulation research, technology transfer, CMC regulatory requirements, and GMP compliance. 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 ...
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