[武汉]鼎康（武汉）生物医药有限公司

岗位描述：
?Understand technical aspects of the job, best practices, and adhere to cGMP compliance.
了解工作的技术方面、实践，并遵守现行GMP规范。
?Management of culture medium and strains.
管理培养基及菌种。
?Draft and execute the method validation protocol for Bioburden, Endotoxin, and Sterility test according to ChP, USP and EP.
起草并执行微生物限度检验、内毒素检验、无菌检验的方法验证方案，符合中国药典，美国药典及欧洲药典要求。
?Communication with client about the gaps and questions of method validation for Bioburden, Endotoxin, and Sterility analysis, and resolve the problems, if any.
与客户沟通生物负载检验、内毒素检验、无菌检验的方法验证的分歧及问题，如有问题，确保解决。
?Handle the deviation and micro data deviation event.
处理偏差以及微生物数据偏差事件。
?Training members of the department and other departments as necessary.
必要时，培训部门成员以及其它部门成员。
?Develop and implement all necessary SOP/test procedures.
开发及执行相关的SOP/检测规程。
?Any other tasks as assigned by the supervisor.
主管分配的其它任务。