北京招聘

The Role:

1.负责GC-MS、LC-MS-MS或者ICP-MS等仪器的维护、保养、基本维修工作；

2.负责起草各种基于各种化合物，生物体基质流体的分析方法开发与验证方案；

3. 完成各种分析测试工作及报告起草，并根据实际项目提供相应的解决方案和技术支持。

1. Responsible for the maintenance, maintenance and basic repair of GC-MS, LC-MS-MS or ICP-MS;

2. Responsible for drafting various methods for the development and verification of analytical methods based on various compounds and biological matrix fluids;

3. Complete various analysis/ testing work and report drafting, and provide corresponding solutions and technical support according to projects.

In this role you will:

1.仪器软硬件：承担起A组（GC-MS、LC-MS-MS）或B组（ICP-MASS）的仪器使用，保养和基本维修工作

2.仪器应用：承担起验证中心可提取物&浸出物的A组或B组的法规符合性研究性分析检测和法规性支持工作；

3.项目支持：完成内部仪器和法规类培训和部分可提取物和浸出物项目的对外客户沟通工作。

1.Instrument software and hardware: undertake the use, maintenance and basic maintenance of instruments in Group A (GC-MS, LC-MS-MS) or Group B (ICP-MASS)

2.Instrument application: undertake research and analysis and regulatory support for regulatory compliance of Group A or Group B extractables & extracts;

3.Project support: complete internal equipment and regulations training and external customer communication for some extractables and extractables projects.

Traits we believe make a strong candidate:

1. 3年或以上在制药或药包材企业QC，R&D部门以及第三方药物检测分析及R&D检测实验室工作经历，其中必须有2年或以上涉及GC-MS、LC-MS-MS或者ICP-MS等仪器的检测分析或R&D工作经历；

2. 热爱仪器分析工作，能够运用excel或origin对测试数据进行处理；

3. 熟悉国内外各中涉及药包材，过滤材料和弹性体的可提取物和浸出物分析检测类法规，包括EMEA,USP,ICH和CP。

1.3 years or more working experience in QC, R & D department and third-party drug testing analysis and R & D testing laboratories of pharmaceutical or pharmaceutical packaging materials companies, which must have 2 years or more involving GC-MS, LC-MS-MS or ICP- Test and analysis of MS and other instruments or R & D work experience;

2. Love instrument analysis work, can use excel or origin to process test data;

3. Familiar with domestic and foreign regulations concerning the analysis of extractables and extractables of pharmaceutical packaging materials, filter materials and elastomers, including EMEA, USP, ICH and CP.

Your success will be measured by:

? 按照部门完成内外服务项目，并不断更新自己的知识和技能。

? Complete internal and external service projects by department, and constantly update their knowledge and skills.

关于Entegris

Entegris是为微电子行业和其他高科技行业提供特殊化学品和先进材料解决方案的领导企业。Entegris通过了ISO 9001认证，在美国、中国内地、法国、德国、以色列、日本、马来西亚、新加坡、韩国和中国台湾设有制造、客户服务和/或研究机构。