SMO Quality Control(QC)
科锐国际人力资源(北京)有限公司
- 公司规模:1000-5000人
- 公司行业:专业服务(咨询、人力资源、财会)
职位信息
- 发布日期:2013-09-18
- 工作地点:北京
- 招聘人数:若干
- 职位类别:药品生产/质量管理
职位描述
KEY ACCOUNTABILITIES:
1、 Be fully responsible for the registration of assigned projects;
2、 Contribute to registration timeline, prepare documentation and submission on schedule;
3、 Follow up the registration and evaluation status in SFDA & CDE;
4、 Answer technical questions from SFDA & CDE;
5、 Be responsible for the sample order, dossier order;
6、 Be responsible for dealing with relative issue on drug quality test in SDA’s lab;
7、 Effectively and clearly communicate with other department;
8、 Report to line management regularly.
JOB-HOLDER ENTRY REQUIREMENTS:
1、 Bachelor's degree (advanced degree preferred) plus at least 7 years of experience in pharmaceutical -industry or clinical-related discipline including at least 5 years clinical research experience.
2、 Good command of English ( written and spoken)
3、 Knowledge of PC (WORD, EXCEL, POWERPOINT)
4、 Interpersonal communication skill
5、 Team player
联系人:贾先生
邮箱:stevenjia@careerintlinc.com
电话:010 59271378