青岛招聘

职位描述：
1. Responsible for schedule the sampling task of raw materials, packaging materials, purified water and soften water.
负责原材料、包材、纯化水和软化水的取样安排。
2. Responsible for the preparation and maintenance of Specifications, Test Method and Test Record of raw materials, packaging materials, purified water and soften water.
负责准备和维护原材料、包材、纯化水和软化水的质量标准、检验方法和检验记录。
3. Responsible for schedule the testing task of raw materials, packaging materials, purified water and soften water.
负责原材料、包材、纯化水和软化水的检验安排。
4. Responsible for review the chemical testing and online documentation on site.
负责现场复核理化检验和实时记录。
5. Responsible for the relative Excel sheet validation and usage in respective team.
负责本组相关Excel数据表的验证和使用。
6. Responsible for maintenance of standard solution, volumetric solutions, reagents, indicators and etc.
负责本组对照溶液、滴定液、试剂和指示剂等的维护。
7. Responsible for the review of the relative logbook for the respective team.
负责本组相关记录本的复核。
8. Responsible for the review of the test record for the respective team.
负责本组相关检验记录的复核。
9. Responsible for the preparation of COA.
负责准备COA。
10. Responsible for the usage and maintenance of column usage logs in the respective team.
负责本组内色谱柱的使用和色谱柱使用记录的维护。
11. Responsible for the method transfers from external vendors and from ARD.
负责来自外部供应商和ARD的方法转移
12. Responsible for the co validation and pharmacopeia method verifications.
负责共同验证和药典方法确认。
13. Responsible for the relative document preparation for the method transfers, verifications and validations.
负责为方法转移、确认和验证准备相关文件。
14. Responsible for the issuance of status labels in the respective team.
负责更新本组的状态标识。
15. Responsible for the training related to the respective section.
负责本组的相关培训。
16. Responsible for the quality notifications in respective team. (OOS, OOT & Deviations & Investigation).
负责本组的质量报告。（OOS、OOT、偏差、实验室调查） 举报 分享

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       宜昌人福出口药品生产基地是宜昌人福为实践“国际化战略”斥资6亿人民币打造的集研发生产和销售于一体的高端仿制药制剂公司，自2013年项目成立以来，已有多个自主研发的产品通过FDA官方认证，并有多个OTC产品实现了在欧美等地的销售。