Senior Quality Compliance Auditor

QA

Your new company

Your new role
  • Perform Supplier Audits in the APAC region
  • Perform Internal BeiGene Audits
  • Provide Quality Compliance guidance of cGMP external manufacturing operations (CMO) as necessary
  • Provide input to Quality Agreement content as needed. Support the process of Quality Agreement implementation and updates into the Global Quality Program
  • Provide Quality compliance guidance and support on quality investigations and change controls
  • Support or provide compliance auditor training.
  • Support health authority inspections and partner audits
  • Support Global Quality Systems and Global Standards implementation in China
  • Assess and revise, as needed, SOPs for GMP Quality functions and identify opportunities to streamline systems and processes
  • Perform duties as assigned to ensure compliance to global and local regulations


What you'll need to succeed
  • Minimum of 15 years pharmaceutical or biotechnology industry GMP experience in a quality and manufacturing function


What you'll get in return

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1232030

职位摘要

职位类型:
长期
行业
Pharmaceuticals
工作地点
Shanghai
专业领域
Life Sciences
参考编号
1232030
关闭日期
5 Feb 2023

咨询我们的专业顾问

请联系负责该职位的专业顾问 Lennie Wang, , 地址位于 Shanghai
Unit 1205-1212, HKRI Centre One, HKRI Taikoo Hui, 288 Shimen Road (No.1)

电话号码: +8602123229787

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