Be responsible for the formulation development strategy and plan of the project, as well as the analysis of the usage mode, mechanism of action, technical indicators, technical feasibility and patent feasibility of the product.
3.67 负责制定制剂工艺开发阶段性目标，拆解工作任务并合理安排组员进行工作。
Responsible for formulating stage goals of purification process development, dismantling work tasks and reasonably arranging team members for work.
Complete the work summary and report, participate in and supervise the formulation, writing and implementation of each plan in the process of process development, write the report after completion, and be responsible for the output results.
5.67 能独立负责制剂工艺开发放大，并能协调相关部门完成相关工作。
Independently responsible for the development and amplification of preparation process, and able to coordinate relevant departments to complete related work.
6.67 负责与客户对接、交流、汇报工作，保证任务的即时、准确、专业性。
Responsible for communicating, communicating and reporting with customers to ensure the promptness, accuracy and professionalism of tasks.
7.67 完成制剂相关项目管理和申报，确保符合注册法规与行业趋势。
Complete preparation related project management and application to ensure compliance with registration regulations and industry trends.
8.67 负责制剂研发成本的核算。
Responsible for the cost accounting of preparation R&D.
Responsible for the management and maintenance of the inspection equipment to ensure that the inspection equipment can operate normally and within the validity period. Responsible for new equipment installation, debugging, calibration, validation and equipment file establishment.
10.67 完成领导分配的其他工作和职责。
Complete other tasks and responsibilities assigned by the leader. 任职资格: 1、微生物学，化学工程，生化工程等理学或生物制药，制药工程等工学学士及以上，硕士优先。 2、至少五年以上从事制剂相关工作（医药固液无菌制剂类工作经验优先）的实践经验。 3、能够阅读相关的英文资料。
