职位描述
职位描述主要从事气相色谱，气质联用的定性和定量分析，结构鉴定，分析方法开发。有多年用气质联用做结构鉴定的经验，了解药典和GMP法规，具有在药厂从事分析检测工作经验的求职者优先考虑。A Sr. Scientist/Supervisor will be responsible for method development, method validation and stability testing of structural chemistry products within a cGMP environment. Must have extensive theoretical and hands on knowledge of structural elucidation of target/lead compounds, synthesis and purification of impurities and degradation products. Will design and conduct appropriate experiments, writing protocols, scientific reports and participating in the interpretation of data, writing protocols and reports in support of structure elucidation and validation studies. Should have knowledge of GMP and regulatory issues (FDA, ICH, USP). Prepare detailed written reports of findings and make oral presentations of project status. Inform the project team leader/department manager on any part not meeting the timeline and work out with the responsible person to change the plan. Must be proactive and creative, willing to learn quickly, well-organized, team players, able to work independently, and should possess excellent communication skills. Will be expected to coordinate the activities of a small group of chemists/scientist. Project management experience and supervisory experience is a plus. Requires MS or Ph.D. Degree with 3+ years of analytical method development experience using analytical instrumentation, including GC and GC/MS. Experience in two or more of these instruments are required. 工作职责：1、熟练的进行一般化学分析、气相色谱、液相色谱、液质联用、气质联用、多级质谱.2、用质谱对样品中未知化合物进行结构鉴定3、能够很好的理解药典（USP、EP）和其他方法和程序，在cGMP，FDA，ICH的相关法规下遵循药典和其他方法进行实验操作。4、编写实验报告，审核药品检验员的实验记录和报告。5、协助部门主管或经理，保证项目的高质量和按时完成。任职资格：3-5年或以上相关实验经验。 具有项目管理经验，能同时进行多个项目，有良好的解决问题的能力和良好的沟通技巧。有较强的主观能动性和创造性，能独立和按时完成工作，同时具有团队合作精神。
