Career Opportunities

Report Writer

Responsibilities:

  1. Ensuring the implementation and supervision of QA system.
  2. Conducting production on-site inspection / in-process control.
  3. Ensuring that the raw materials, packaging materials and intermediate, bulk and finished product are approved or rejected according to defined procedure or specification.
  4. Ensuring medicinal products are stored, distributed and subsequently handled as the requirements of defined procedure throughout their shelf life.
  5. Ensuring Specifications, sampling instructions, test methods and other procedures related with GMP operation are effective before using.
  6. Supporting the validation activities and ensuring that the appropriate validations are done according to VMP and defined procedures.
  7. Reviewing batch record and ensuring the operation complies with defined procedures.
  8. Reviewing test records and reports and issue CoA for project and product.
  9. Coordinating deviations, making sure the corrective or preventative actions are carried out and documented the trace system to prevent deviations from re-occurred.
  10. coordinating change control, making sure any change are documented according to defined procedure and all impacted items are investigated and evaluated, making sure the proposal changed implement as the requirements of pre-defined protocol.
  11. Taking part in the investigation, documentation and communication of GMP nonconformity.
  12. Conducting internal audit and routine inspection.
  13. Coordinating vendor audit and on-going management.
  14. QA related SOP’s drafting, revision and review.
  15. Providing GMP/Quality Assurance related training.
  16. Periodical quality evaluation with other departments.
  17. Any job and responsibilities assigned by QA director.

Minimum requirements:

  1. BS or MS degree in a science discipline with experience or training in Analytical, Pharmaceutical, or equivalent experience.
  2. Strong communication skills, both written and verbal, and outstanding interpersonal skills are essential job requirements.
  3. Must be able to openly share information and work in a team-oriented manner in order to accomplish performance objectives.

Send your C.V. with salary requirements to:

hr@wuxiapptec.com
Fax: 86-21-50461000
Mail: Human Resources
WuXi PharmaTech Co., Ltd
No. 1 Building, #288 FuTe ZhongLu
WaiGaoQiao Free Trade Zone
Shanghai, China 200131

Visit us at www.wuxiapptec.com.
Direct applicants only - no agencies please.

WuXi AppTec Co., Ltd. is a NYSE listed public company based in Shanghai, China. We offer global pharmaceutical/biopharmaceutical companies diverse outsourcing services in combinatorial, medicinal, synthetic chemistry and manufacturing of API’s and finished drug products for preclinical and clinical trials. Our clients include over 80 leading global pharmaceutical and biotech companies in the U.S., Europe and Japan.

WuXi Apptec Co., Ltd. welcomes overseas scientists to join us. We offer you a highly competitive compensation and full benefits package along with an exciting world-class research environment.

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