職位描述
職位描述主要從事氣相色譜，氣質聯用的定性和定量分析，結構鑒定，分析方法開發。有多年用氣質聯用做結構鑒定的經驗，了解藥典和GMP法規，具有在藥廠從事分析檢測工作經驗的求職者優先考慮。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. 工作職責：1、熟練的進行一般化學分析、氣相色譜、液相色譜、液質聯用、氣質聯用、多級質譜.2、用質譜對樣品中未知化合物進行結構鑒定3、能夠很好的理解藥典（USP、EP）和其他方法和程序，在cGMP，FDA，ICH的相關法規下遵循藥典和其他方法進行實驗操作。4、編寫實驗報告，審核藥品檢驗員的實驗記錄和報告。5、協助部門主管或經理，保證項目的高質量和按時完成。任職資格：3-5年或以上相關實驗經驗。 具有項目管理經驗，能同時進行多個項目，有良好的解決問題的能力和良好的溝通技巧。有較強的主觀能動性和創造性，能獨立和按時完成工作，同時具有團隊合作精神。
