北京招聘

Responsibilities:

• Complete the assigned routine inspection of sample, issue the reliable analytical report in reasonable lead time.
• Obey the requirement against global GMP standards and China GMP requirement, to improve the compliance level.
• Implement the maintenance and calibration of assigned instruments
• Report the abnormal status, unexpected results to supervisors with initiative and in time.
• Guide colleagues to fulfill analysis tasks.
• Complete the assigned analysis method validation.

Requirements:

• At least 5 years' experience in Quality Control Unit of major or joint venture Pharma Company
• Bachelor of Science Degree or above, Pharmacy, Chemistry, Biochemistry and equivalent
• Professional knowledge of physical & Chemical analysis
• GMP implementation experience and sense
• Project management skills
• Fluent in both written and spoken English and good PC skill(above CET-6)

上海罗氏制药有限公司成立于1994年，是抗肿瘤、抗病毒、移植等关键领域的市场领导者。在大型跨国药企中，我们率先在中国建成了包括研究、开发、生产、营销等环节在内的完整的医药价值产业链。罗氏中国正向着成为罗氏全球第三个战略中心的目标迈进，以实际行动践行在中国长期发展的承诺。

我们始终以患者为中心，致力于帮助患者从根本上延长生命和改善生活质量。目前，罗氏在华拥有16个产品，覆盖8个治疗领域。我们与政府、医疗机构以及非政府组织等社会各界多方携手，共同探索创新的合作模式，通过一系列有影响力和可持续的举措惠及更多的中国患者。

更多罗氏中国信息，请登陆罗氏官网或访问罗氏招聘公众号。