[武汉]鼎康（武汉）生物医药有限公司

职位描述：
? Oversee the activities related to late phase process development, process characterization, and process validation, as well as BLA readiness.
? Write, revise and review protocols and reports related to process characterization, and process validation in compliance with all applicable regulations, including but not limited to process validation, column/membrane/system cleaning validation, resin/membrane lifetime validation, etc.
? Write, revise and review other related documentation as necessary to support late phase product development and BLA application.
? Assist on the activities related to process and method tech transfer, process scale-up and cGMP manufacturing.
? Take on other tasks as needed by MSAT or the company.
? Build the future of the organization through developing employee’s knowledge, understanding, and skills to improve performance and expand abilities
? Ensure collaboration and commitment between MSAT and other departments in order to meet internal and external expectations