北京招聘

岗位职责：
1. Support analysis test of FP, ST and FUST according to company's Control procedure and local registration analytical methods strictly, supply accurate results in time.
严格按照公司控制程序和本地注册的分析方法来支持成品和稳定性分析。
2. Support analysis for process validation of product.
支持产品工艺验证分析。
3. Support special analysis investigation, method development and validation.
支持特殊调查、分析方法开发和验证。
4. Support the work of other team of product test.
支持成品检验工作。
5. Support the qualification and requalification for all QC lab equipment according to relevant local SOP.
根据相关的本地标准操作规程支持所有实验室设备的确认及再确认。
6. Support the calibration and maintenance for all QC lab equipment according to relevant local SOP.
根据相关的本地标准操作规程支持所有实验室设备的校准和维护。
7. Coordinate the supplier’s engineer to repair the QC lab equipment.
协调厂家工程师上门维修实验室设备。
8. Conduct works to be required by QC coordinator.
完成质量控制协调员分配的工作任务。

任职资格：
1. A Bachelor degree in Chemical Technology/Pharmacy and 1 year's experience in similar position hands-on experience in HPLC, UV, etc. Good data analysis skills. Be proficient in using the computer software such as Word, Excel and etc.
在药学，化学或分析专业本科学历，有两年以上相似岗位的工作经历，操作过HPLC ，UV 等，有较好的数据分析能力，熟练操作word，excel 等软件。
2. Be able to read and understand English documents.
能够阅读和理解英文文件。
3. Familiar with regulatory requirements (GMP/GLP, etc.)
熟悉相关法规，例如GMP/GLP等。
4. Strong analytical and problem-solving skills.
有较强的分析和解决问题的能力。