[武汉]鼎康（武汉）生物医药有限公司

岗位描述：
? Provide daily operation support in QC laboratory, understand technical aspects of the job, best practices, and adhere to cGMP compliance.
QC实验室进行日常实验操作，理解工作的技术原理，最佳做法，并遵守cGMP合规性；
? Develop and qualify potency assay and impurity assays such as HCP, DNA, and Residual ProA methods to implement at GMP QC groups following ICH/USP/EP/CP guidelines.
根据ICH/USP/EP/CP指南开发和验证生物效能实验和杂质分析实验方法，例如HCP，残留DNA和残留ProA；
? Develop and implement all necessary SOPs, perform analysis of in-process and finished formulations according to SOPs, work to relevant cGMP standards testing in process checks and stability samples,
撰写和补充所有必须的SOP，根据SOP对中间样品和制剂进行分析检测；依照相关cGMP标准进行中间样品和稳定性样品的检测，
? Perform moderate data analysis and trending, document work according to GMP and notify management;
进行适当的数据分析和趋势分析，根据GMP进行文件工作并通知管理人员；
? Other work arranged by superior leaders.
上级领导安排的其他工作。