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
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