苏州招聘

职位描述：
1. Be responsible for performing routine tests for environment air /compressed air /water system for monitoring and validation purpose.
负责执行对环境空气/压缩空气/水系统的日常监测或验证测试。
2. Be responsible for sampling, receiving and disposal of materials in QC lab.
负责对QC实验室物料的取样、接收及处理工作。
3. Be responsible for preparation and watching for post-production cleaning verification.
负责生产后清洁验证的准备及监督工作。
4. Be responsible for media preparation and microorganism control.
负责培养基的准备及菌种的管理控制工作。
5. Participate in 6S work in lab and maintain the cleanliness of test area, glassware and equipments, especially the disposal of hazardous waste in QC lab.
参与实验室的6S工作并维持测试区域，玻璃仪器及设备的清洁，尤其是QC实验室有害废弃物的处理。
6. Assist Microbiologist in drafting/revising microbial test related SOPs/TMs.
协助微生物师起草/修改微生物相关的测试程序及测试方法。
7. Other tasks assigned by Superior.
其他上级安排的工作。

岗位要求：
1. Bachelor or above degree in Microbiology or relative.
微生物学或相关专业本科及以上学历。
2.1+ year experience related to Pharmaceutical QC lab experience, and excellent graduating student is also welcomed.
1年以上制药QC实验室经验，应届毕业生亦可。
3. Basic microbiology technical knowledge especially Morphological Characteristics and Identification of bacteria.
微生物基础知识,尤其是细菌的形态和鉴别。
4. Basic microbial test skills and aseptic technique.
基本的微生物测试技能。
5. cGMP knowledge for microbiology lab and chemical lab in the pharmaceutical industry.
药品行业微生物/化学实验室cGMP相关知识。
6. Basic Microsoft office operation skills.
基本掌握办公软件的操作。
7. Self-starter, disciplined, safety oriented.
做事主动、安全可靠。 举报 分享

Amerigen Pharmaceuticals is a multinational company with established development and manufacturing platforms aimed at providing high-quality generic pharmaceutical products. Its headquarter is based at New Jersey, US.
爱美津制药是一家集研发和制造于一体的跨国公司，旨在向美国提供高质量的仿制药品。总部位于美国新泽西州。

With pharmaceutical assets and science-based expertise in the United States and abroad, Amerigen is able to provide quality products at competitive prices along with unmatched customer service.
凭借在美国和海外的制药资产和技术专家队伍，爱美津致力于提供高品质产品、有竞争力的价格和无以匹敌的客户服务。

At the end of 2007, Amerigen has successfully completed the acquisition of an oral solid dose manufacturing facility in Suzhou Industrial Park, China and established Suzhou Amerigen Pharmaceutical Co., Ltd.
2007年底，爱美津完成了在中国苏州工业园区的口服固体制剂生产厂的收购，并成立了苏州爱美津制药有限公司。
 
The milestones of Suzhou Amerigen are as follows:
苏州爱美津制药的里程碑如下：

2007 Suzhou Amerigen was established
      苏州爱美津成立
2008 First US regulatory filing
      首次获得美国法规文件受理

2009 First US FDA PAI & General Inspection
      首次美国食品药品监督管理局上市批准和常规检查

2010 Received US FDA approval for bulk tablet manufacturing
      获得美国食品药品监督管理局的批准生产大包装片剂

2012 Passed CFDA Re-Inspection (GMP 2010 version)
      通过中国食品药品监督管理局再次检查-新版GMP (2010版)

2013 Passed US FDA Inspection –Recommended approvals on four ANDAs
      通过美国食品药品监督管理局检查- 4个简化新药被推荐批准

2014 Launched US Product and re-introduced China Products
      产品在美国市场上市, 中国市场产品恢复生产。

2015 Passed US FDA Inspection on Data Integrity
      通过美国食品药品监督管理局针对数据完整性的专项检查