武汉招聘

岗位描述：
? To participate in literature screening, quality research, prescription screening and technology transfer involved in the preparation project;
参与制剂项目的文献调研、质量研究、处方筛选及技术转移；
? To independently screening and optimize the formulation process of different dosage forms according to domestic and international quality requirements and GMP requirements;
按国内国际质量要求及GMP要求，独立开展不同剂型的处方工艺筛选和工艺优化研发；
? To complete the pilot scale-up of the formulation, preparation of the pilot product and stability study;
完成制剂的小试放大，中试产品的制备、稳定性研究；
? Familiar with the properties of excipients, formulation process and the use of instruments and equipment;
熟悉制剂各辅料性质、制剂制备工艺和仪器设备的使用；
? Familiar with the methods and instruments of drug analysis and be able to study the quality of formulation according to requirements.
熟悉药物分析的方法及仪器，能根据要求进行制剂质量研究；
? To conduct formulation research and make relevant original records according to relevant specifications, organize and file data, assist and participate in the preparation of declaration data;
按照相关规范要求进行制剂研究并做好相关原始记录，进行资料的整理编写归档，协助并参与申报资料的撰写；
? Laboratory maintenance, calibration, operation, maintenance and maintenance of formulation equipment shall be carried out and operated according to SOP.
实验室的维护、制剂设备的校正、操作、维护、保养，按SOP执行和操作；
? Work closely with relevant departments to ensure the smooth progress of the project.
与相关部门紧密合作，确保项目的顺利进展；
? Other related work arranged by superior supervisor.
上级主管安排的其它相关工作。

鼎康生物是一家领先的CDMO公司，可提供一站式的CMC解决方案，支持从早期药物开发到后期临床研究和商业化cGMP生产。鼎康引进了全球***模块化生物制药工厂Kubio；为客户开发的多个产品已经在全球20多个国家进行临床试验。在不久的将来，鼎康生物总产能将超过140,000L。我们承诺通过技术和生产创新，使全球患者都能负担得起具有国际标准的生物药物，提高治疗水平以改善人类健康。