招聘职位
- Plant Engineer（某瑞士独资制药公司）
- Process Safety Manager（某瑞士独资制药公司）
- 财务分析
- Mixing Process Engineer
- Mechanical Engineer
- Safety and Security Officer
- OH Specialist 职业卫生专员
- Senior Accountant / Accountant
- Maintenance Manager
- Plant Engineer (Solvent Recovery Plant)
- Effluent Treatment Engineer
- Quality System manager
- Senior Process Engineer(高级工艺工程师）
- Senior Project Engineer
- Mechanical facilities Engineer
- ZJG Finishing Plant Instrument Engineer
- ZJG Finishing Plant Reliability & Integrity Engineer
- PLANNER/SCHEDULER - 某美资化工企业
- ZJG Process Engineer-某美资化工企业
- Production Manager(上海知名德资化工企业，世界五百强）
- Civil Engineer-某美国独资公司
- Assistant Maintenance Manager-某法资化工企业
- Chemical Engineer-某瑞士独资制药公司
- Environment Engineer 环境工程师-某法国独资公司
- 化工操作-欧美新建项目
- Safety Lab Chemist-某瑞士独资制药公司
- QA Manager-某瑞士独资制药公司
- Chemist II-某美资企业
- Researcher-A Famous Finland Paper Mill
- 淬火剂销售经理-某化学品贸易公司
- Pulp Researcher-某知名芬兰造纸公司
- Polymer Process Manager-某法资化工企业
- Organic Peroxide Process Engineer-某法资化工企业
- Polymers Monomers Process Engineer-某法资化工企业
- Chemical Engineering Manager-某法资化工企业
- Fluoropolymers R&D Engineer-某法资化工企业
- Polymer Engineer-某知名芬兰造纸公司
- Technical Supervisor-A Famous American Corporation
- Plant Engineer- A Famous German Chemical Corporation
- Injection Molding Engineer- A Famous German Chemical Corporation
- 实验室分析员
- 化工操作工
- 化工操作技术员-某外资化工企业
- Manager, Quality and License-某世界500强德资企业
- Process Engineer-Automation-某知名德资化工企业
- QA/QC Manager - QA/QC Engineer-某知名德资化工企业
- Mechanical Engineer-某知名德资化工企业
- Production Manager-某知名德资化工企业
- Plant Engineer-Electrical & Mechanical-某知名德资化工企业
- Day shift Leader-某知名德资化工企业
- Specialist of Facility & Security Management
QA Manager-某瑞士独资制药公司
| 职位编号： | 1783019 | 招聘日期： | 2014-08-25 ~ 2014-11-25 | 招聘部门： | 不限 |
|---|---|---|---|---|---|
| 工资待遇： | 面议 | 工作地点： | 江苏-苏州市 | ||
| 招聘人数： | 1人 | 学历： | 本科 | 工作年限： | 3年以上 |
| 性别要求： | 不限 | 年龄要求： | 18岁到60岁 | 所在地区： | 不限 |
| 职位描述： | 1. Manage equipment qualification and IT system validation projects and approve related documents including Validation Master Plan, Change control and Deviations. Act as e-Compliance Manager for TRD CN.
2. Review of GMP relevant documents such as manufacturing masters and control procedures, executed batch records, specifications, test methods and analytical records for GMP compliance. With training and specific delegation may also approve relevant documents. 3. Recognize deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up. 4. Establish and maintain QA documentation systems such as applicable Quality Manual and SOPs. 5. Support TRD CN quality initiatives, e.g., quality risk analysis, quality plan. Act as a QA representative on site quality improvement projects. 6. Support internal audits by QA. Assume QA responsibility in the management of third party according to applicable SOPs and ensure that material manufactured for *** is in compliance with *** Standards. 7. Be a valuable team member of Quality organization and develop self and others through close teamwork and cross functional activities such as collaboration and communication with Line Units. Education: Minimum: A bachelor degree in related scientific field Desirable: Advanced degree in laboratory, manufacturing, pharmaceutical or relevant discipline. Languages: Fluent in English and Chinese Experience: Minimum 3 years of relevant experience in laboratory, manufacturing or pharmaceutical development and/or Quality Assurance and Quality Control. Working under GMP operations is a plus. |
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| 面试地址： | 江苏常熟市海虞北路19号亿源世纪广场A栋27楼03室 | ||||
联系方式 |
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| 联系人： | 胡先生 | Email： | （请通过系统发送求职意向） | ||
| 联系电话： | |||||
