| 查看: 1342 | 回复: 7 | |||||||||||||||
| 当前只显示满足指定条件的回帖，点击这里查看本话题的所有回帖 | |||||||||||||||
jennifer9707新虫 (初入文坛)
|
[交流]
液体制剂科学家（大分子合成经验）
|
||||||||||||||
液体制剂科学家 在学校或工作中有大分子合成经验； 学历：硕士必须3年以上工作经验；博士可以无工作经验的毕业生； 语言：英文听说读写熟练 |
回复此楼» 猜你喜欢
结合人工智能，周易传统文化，filecode打分制来了，3分以上希望很大。
已经有4人回复
-
2019年青年基金涵评意见，大家看看几个A，几个B?
已经有11人回复
-
重要来源：本周末出结果
已经有5人回复
-
FileCode能看出啥？
已经有23人回复
-
应该是93bebmhtak前后十一个字符比较关键
已经有36人回复
-
关于Filecode分析方法
已经有9人回复
-
不应该看fileCode
已经有6人回复
-
好奇怪的filecode
已经有6人回复
-
长年满屏的广告，版主太不责任了。基金也等的急
已经有4人回复
-
filecode
已经有15人回复
» 本主题相关价值贴推荐，对您同样有帮助:
- 过程工程所2011年招聘启事
已经有9人回复
zhengyi
木虫 (著名写手)
- 应助: 0 (幼儿园)
- 金币: 3917.5
- 散金: 219
- 红花: 2
- 帖子: 1894
- 在线: 745.2小时
- 虫号: 138089
- 注册: 2005-12-18
- 专业: 化学生物学与生物有机化学
3楼2013-08-14 08:04:52
2楼2013-08-13 23:36:25
xiaoyuerxiao
木虫 (著名写手)
五
- 应助: 11 (小学生)
- 金币: 1947.5
- 散金: 15
- 红花: 9
- 帖子: 1203
- 在线: 621.8小时
- 虫号: 920940
- 注册: 2009-12-05
- 性别: GG
- 专业: 合成药物化学
4楼2013-08-14 09:17:07
jennifer9707
新虫 (初入文坛)
- 应助: 0 (幼儿园)
- 金币: 51.5
- 帖子: 48
- 在线: 14.6小时
- 虫号: 2499502
- 注册: 2013-06-07
- 专业: 药物代谢与药物动力学
|
Responsible for the development and characterization of parenteral formulations, with the emphasize on biologics in the Centre of Pharmaceutical Sciences under the Discovery Center of China R&D and SA. The incumbent is expected to manage the operation of the formulation lab and to conduct the formulation activities for various parenteral dosage forms, such as liquid, lyo, suspensions, microspheres and nano-crystals. He/she is also expected to work closely with the manufacturing facilities in China to ensure the timely and smooth scale up and technical transfer. The incumbent will facilitate the verification of noval formulations and processes in a due-diligent team. The incumbent is responsible for the design, conduction, supervision, and reporting of studies that are carried out internally and in contract labs. He/she is responsible for the ensuring compliance and integrity of the studies. • Develop liquid, lyophilized, micronized, and nano and sustained release parenteral formulations of large and small molecules. • Preformulation characterization of new formulations using various lab instruments (e.g. HPLC, CE, UV, DSC, ITC, CD, DLS/SLS, Zeta, Rheometer, etc.). • Provide data and justification for NCE declaration, CTA, BLA and NDA submissions for filing in China. • Formulate stable dosage forms consistent with preclinical and clinical needs. • Evaluate new excipients or platforms to modify solubility and/or stability. • Identify and analyze degradation products and possible degradation mechanisms in formulations. • Write technical reports and present scientific results at internal and external meetings. • Coordinate the work of technical personnel with a special regard to accuracy and reliability of their data. • Ensure the adherence to SOPs and policies. • Train and/or provide work direction to research associates and interns. • Maintain and enforce safety regulations and cleanliness in the work area • Work closely with the manufacturing facilities in China to ensure the timely and smooth scale up and technical transfer Qualifications • Candidate must be a BS with 5+ years, M.S. with 2+ years or a Ph.D with 0+ years of industrial experience in Biochemistry, Engineer, Chemistry, Pharmaceutics or one of the related disciplines • The candidate must be willing and able to work in a laboratory environment • Detail-oriented • Good problem solving capability • Experience in working in a Chinese-speaking country is required. • Strong oral and written communication skills • Good planning and tracking skills |
5楼2013-08-14 09:20:50
