1.Responsible for preformulation support to our promising pipeline of biotherapeutics, planning and executing developability assessments 负责我们有前景的生物药的处方前研究，计划并进行可开发性的评估 2.Hands-on, laboratory-based role that supports the development of lyophilization for therapeutic protein formulations. Develop lyophilization cycles & processes to increase stability of the drug products. 在实验室领导进行新的蛋白药物的冻干制剂处方开发，开发冻干循坏工艺等提高药物的稳定性。 3.Stability testing and characterization of routes of degradation of proteins in liquid and lyophilized formulations under accelerated temperature, refrigerated storage conditions and under agitation and freeze-thaw stresses. 蛋白的水针制剂和冻干粉的稳定性测试以及降解途径的分析，包括加速试验、长期实验以及振荡、冻融挑战实验 4.Good interpretation of biophysical instrumentation (DSC, FTIR, CD, DLS etc.) data. 对于生物物理相关设备（差示扫描量热仪，傅里叶变换红外仪，圆二色光谱仪，动态光散射仪等）有较好地理解。 5.Support of Drug Product manufacturing may be performed, which include process robustness and tech transfer activities. 支持制剂成品的生产，包括生产过程的稳定性和技术转移。 6.Review analytical data for completeness and correctness. 审核分析数据的完整性和正确性。 7.Write formal reports for inclusion in regulatory filings and support the generation of appropriate responses to questions from regulatory authorities. 撰写用于申报材料的正式的报告文件并支持和书写合适的反馈来回答监管部门的问题。