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无工作经验 -
本科 -
招1人 -
11-09 发布
- 五险一金
- 补充医疗保险
- 交通补贴
- 餐饮补贴
- 定期体检
- 年终奖金
职位描述
职位描述： Job category: QA departmentOutsourced to global leading company.Prefer 1-2 years related medical work experienceGood communication skill and fluent English.Good GCP knowledge.Please feel free to contact me if any questions. Thanks!jenny.zhang@docsglobal.com以下为我司对该人员的任职要求，供您参考。1. Assist for management of controlled documents, maintenance updating of online controlled documents. 协助公司受控文件的管理，维护在线受控程序文件的更新。2. Review Controlled Documents status regularly, manage the expire/obsolete process of controlled process. 执行公司内受控文件的定期更新检查，管理受控文件的过期及更新流程。3. Support the training of controlled documents. 协助受控文件的更新。4. Communicate and monitor the implementation of local&global case(inquiry and complaint) documentation quality requirements 协助沟通和监测本地及总部事件(问询及投诉)记录质量要求在中国的执行5. Review and approve the product quality compensation request 协助复核及批准产品质量补偿申请6. Quality Documents & Records Control. Keep records. Have clear filing and maintain of all documents. 质量文件、记录的控制，文件分类归档，保留完好 职能类别： 药品生产/质量管理 医疗器械生产/质量管理
联系方式
南京西路288号创兴金融中心
公司信息
ICON Clinical Research-- a top global CRO company. For more details, please kindly see our website - http://www.iconplc.com/
