1、  本科以上学历；

2、  具有5年以上制药企业QA管理经验；

3、  丰富的工艺、设备、纯水系统等验证经验；

4、  熟悉GMP、CGMP、FDA、TGA等认证标准；

5、  熟练的英语沟通能力。

Job Description:

Quality Engineer belongs to The Quality & Validation Assurance in Tianjin office.

-        Working with a range of quality issues in capital investments projects within the pharmaceutical and biotechnology industry.

-        Main responsibility is to assure that the projects are uted efficiently and all customer and health authorities’ requirements are fulfilled.

Qualification:

-  National and international GMP knowledge.

-  Validation experience.

-  ISO 9001:2000 knowledge.

-  Minimum a Bachelor’s degree in the relevant field.

-  Minimum 5 years related work experience in pharmaceutical or biotechnology industry.

-  Fluent in English – both oral and writing.

Other Requirements：

• Accountable for results with proactive attitude

• Creative, self-motivated, actively participate in specific initiatives and promote positive company culture

• Open-minded and ready for change

• Cooperate and collaborate with business partners with good teamwork spirit

• Customer focus, understand and satisfy internal and external customers

• Continuously improve

• Excellent communication, negotiation and interpersonal skills in English and Chinese

• Detail-oriented with good planning and organizing skill

• Provide high quality solution for customer and work in an efficient and timely manner