CLIENT PROFILE

 

我们的客户是一家美资知名生物制药企业，在上海开办的分公司迄今已有20多年。公司规模较大，其业务主要覆盖在大中华地区，在国内各大城市拥有多家独资或合资企业。公司业务包括多类固体制剂、生物制剂的研发、生产、销售、进口，主要产品包括一些天然产品提取物及其合成类产品，同时也会涉猎环保科技和高科技化工等多个领域。

 

Position: QA Supervisor

 

Responsibilities:

• Undertake and manage Quality investigations at the various OEM’s e.g. broken tablet investigations at one of OEM. Vitamin D poor mixing at other OEM etc.

承担和管理各种各样的OEM工厂的质量调查，例如：某个工厂的断片调查，另一个工厂的VD混合不匀的调查等

• Handle with relevant quality complaint from Australia Market.

处理有关澳大利亚市场的质量投诉

• In the position, you will be reporting directly to the Regional Quality and Compliance Manager.

向澳大利亚区域质量经理汇报

 

Candidate Requirements:

• To have 3 – 5 years experience in pharmaceutical manufacturing or scale-up support or possibly some sort of R&D formulation (preferably film coated tablets) experience.

3-5年药厂生产或中试放大或制剂研发工作经验

• Demonstrated involvement in root cause analysis and preventative actions (as a result of customer complaints or direct manufacturing experience).

参与客户投诉或生产偏差根本原因调查与分析经验

• Basic knowledge in nutritional supplement or pharmaceutical tablet formulation and/or manufacturing methods.

药品或保键品制剂生产基本知识

• Have good communication and literary/reporting skills.

良好的书面及口语交流技能

• Preferably have medium to high level English skills.

具备中等程度以上英语水平

• Allowing you to explore and understand more of the international requirements and regulations.

探索与了解国际法规需求

• You should be willing to perform short trips to domestic OEM sites to assist in implementation of preventative actions where required.

能够适应国内短途出差

 

Please send your updated CVto:r.chen@excelhro.com