Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • Shanghai

Description

•Establish analytical method & documents and give support to QC to ensure QC test is based on GMP/GLP-compliant documents and to manage replenishment of reference substances/critical reagent/cell. 
为QC建立分析方法&文件并给与支持,使得QC的测试基于符合GMP/GLP的文件,并管理标准品/关键试剂/细胞。
•Support to Regulatory on analytical issues and coordinate between Regulatory and Technical for technical registration requirement to achieve smooth approval of registration by authorities.
给予注册部在分析事务方面的支持,在注册部与技术部之间进行协调,使得注册事务能顺利批准。
•Continuous improvement of process and bio-technology to drive business support.
为支持业务,对流程与生物技术进行持续改进。

About the company

Roche is a Swiss global health-care company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange.

The company headquarters are located in Basel and the company has many pharmaceutical and diagnostic sites around the world – including: Tucson, AZ; Pleasanton, CA; Vacaville, California, Oceanside, California, Branchburg, NJ; Indianapolis, Indiana; Florence, South Carolina; and Ponce, Puerto Rico in the US; Welwyn Garden City and Burgess Hill in the UK; Clarecastle in Ireland; Mannheim and Penzberg in Germany; Mississauga and Laval in Canada; Shanghai in China; Mumbai & Hyderabad in India; São Paulo and Rio de Janeiro, Brazil; Segrate, Milan in Italy; Johannesburg in South Africa; Karachi, Islamabad and Lahore in Pakistan. There are 26 manufacturing sites worldwide.

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