The Position title is Sr. Associate Document Specialist.
Major Task:
Perform in GD Asia the global formal review process for newly registered Internal Reports.
Contribute in concert with Document Management groups in Germany and US around the clock DM expertise.
Perform user support to secure compliant usage of BHC Document Management Systems.
Continuously improve document quality in ShareDoc.
Requirments:
Education:
Bachelor in medicine, life sciences, or medical computer science or
comparable experience
Experience:
- At least 1 years in the pharmaceutical industry, preferably in global
regulatory affairs would be of advantage
- Knowledge of regulatory and other R&D business processes
- Basic understanding of IT in relation to regulatory requirements and
health authority guidelines
General skills:
- Structured and process oriented thinking, organizational
talent, persuasiveness, ability to work under pressure
- Team oriented, ability to contribute ideas to a team based working
environment
- Fluent in English. Mother tongue Chinese, another language,
preferably German, is desirable
简历或咨询相关问题，请发邮件到airry.s@hotmail.com
谢谢！
发表于 2013-6-25 17:28:29
