杭州招聘

Mission职能:

To execute Third Party GMP audits to pharmaceutical (API and Dosage Forms) companies in China and other Asian countries

为其他亚洲国家的生物制药公司提供第三方审计服务(原料和制剂领域).
· Technical support to develop Chinese consultancy market.
为中国咨询顾问市场提供技术支持.

Required training and knowledge 培训和认知要求:
· bachelor degree in chemical, pharmaceutical or biotechnology.
至少本科学历,化学，制药或生物技术专业.
· More than three years experience in manufacturing or quality areas in an APIs or Dosage Forms pharmaceutical companies, preferable in a multinational (European, USA) environment.
在药品或原料药的制药生产或质量方面具有至少三年以上的质量管理，验证管理经验,在外资企业(欧洲、美国)工作经历者尤佳.

Knowledge in related Quality Systems like ISO13485, 21CFR 820, or GAMP5.
具备ISO13485, 21CFR 820, or GAMP5等质量体系知识。
· Willing to travel frequently
可以频繁出差。
· Good command of English level
熟练的英语沟通