工作职责:
从事原料药的物理化学研究，包括但不局限于溶解度研究、稳定性研究，HPLC方法开发。

2. Plan and execute analytical method development and validation for drug substances and products， stability study, and study reports..

从事原料药和药物制剂分析方法的开发和验证，稳定性研究, 撰写研发报告。

3．Develop new formulations （such as nano-particles, solid dispersion, microemulsion）for preclinical studies to improve bioavailability.

开发新的制剂(如纳米微粒，固体分散剂，微乳)用于临床前动物研究

4. Assume responsibility for assigned instruments, maintaining them in proper calibration and working order according to the appropriate SOP; perform calibrations as assigned.

对分析仪器按照标准操作规程维护和校准并保持日常运作，对仪器进行校验。

5. Function as project manager role in preformulation development projects under the minimum instruction of the supervisor.

在主管指导下，作为项目经理承担责任。

6. Quick adaptability to new technical advancement and be a technical leader in certain areas.

快速适应新技术发展，并在相关领域作为技术带头人。

任职资格:
1. M.S. or Ph.D. degree in pharmaceutical science, pharmaceutical analysis, analytical/physical chemistry, physical pharmacy or other directly-related science disciplines.

药学，药物分析，分析化学，物理化学，物理药学或其它相关专业， 硕士或博士学历。

2. Familiar with analytical techniques, especially HPLC; Experience with solid-state characterization, analytical techniques is desirable.

熟悉常用分析方法，特别是HPLC。有固态表征仪器和分析技术，及其它处方前研究分析仪器的知识及经验者优先。

3. Experience in formulation/dose development and preformulation development is helpful but not required..

熟悉或者有制剂开发和处方前研究经验者优先。

4. Outstanding communication， both written and verbal, skills in English. Good interpersonal communication skills.

较强的英语口语和写作能力；良好的沟通能力。