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Typical Accountabilities Responsible for establishing study and trial level V2V process. Establish cell therapy site qualification criteria and conduct technical on-site assessment. Responsible for developing V2V related study and trial documents, creating apheresis and product administration
Typical Accountabilities 主要职责 Qualification and Validation 确认和验证 To update SVMP and ensure the visibility of validation plan execution status across the site; 更新工厂验证主计划，确保其执行状态的可见性； To coordinate with the site QSR implementation; 协调工厂QSR的实施 To give the training on
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