• 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/

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