苏州立生医药，工作地点在独墅湖的纳米科技园A座

招聘人数：6到8名，待遇从优

投递邮箱：lexenhr@126.com，17312567960，张薇。简历投放邮箱和联系人。

质量合规助理岗位职责要求

QualityComplianceAssistantJob Description

岗位描述：

Position Brand Description:

支持质量合规部门建立质量体系，进行文件整理/编写/翻译/分发等工作。

Support Quality Compliance Team to establish Quality System, with documentation management, edition, translation, distribution, etc..

主要职能：

Key Objectives/Deliverables:

协助主管建立质量体系，对文件进行整理和编辑，按照固定的格式进行更新，并将相应的中文或英文进行互译，整理成文；

Support supervisor to establish the quality system, including sort, edit documents according to required format and translate into Chinese or English as required.

负责质量体系文件的审核流转，确保文件在既定时间内被审核和批准；

Responsible for quality system document routing process to ensure the timely completion for review and approval cycle;

负责受控文件的分发回收，并确保受控文件清单的实时更新以及其可追溯性；

Responsible for controlled documentation distribution and return process and ensure the controlled document list timely updated with its traceability.

完成主管要求的与质量管理相关的事项。

To perform other tasks related to QA.

基本要求：

BasicRequirements:

本科学历，药学化学或相关学科

Bachelor, majored in pharmaceuticals, chemistry or related sciences

英语六级，能流利的听说读写

English level with CET-6 Certificate and fluently in listening, speaking, reading and writing.

其他要求：

Additional Preferences:

None