工作职责:
1. 从事符合GLP要求的生物大分子药物的生物样品分析，为大分子药物药效动力学、药代动力学、毒代动力学研究提供数据支撑We are engaged in biological analysis of macromolecular and micromolecular drugs that meet the requirements of GLP, and provide data support for the study of pharmacokinetics, pharmacokinetics and toxicokinetics of macromolecular and micromolecular drugs
2. 生物样品分析方法开发、方法确认、方法验证和样品分析工作Biological sample analysis method development, method qualification, method validation and sample analysis work.
3. 及时按照相关要求起草、完成和保存实验分析记录和文档Draft, complete and maintain experimental analysis records and related documents in a timely manner according to relevant requirements
4.对于给定的项目必须遵循相关GLP法规要求，实验数据、记录等也要严格遵循相关法规For a given project, relevant GLP regulations must be followed, and experimental data, records, etc. must also strictly comply with relevant regulations.
5.遵循公司SOP开展相关分析工作，能够熟练使用、维护以及修理相关仪器， 能够完成实验记录、报告、数据总结的准备和递交Follow the company's SOP to carry out relevant analysis work, be able to skillfully use, maintain and repair relevant instruments, and be able to prepare and submit experimental records, reports and data summaries.
6.遵守相关法定义务，遵循实验室环境健康安全政策，维护工作台面整洁，正确使用有相应权限的仪器设备Comply with relevant legal obligations, follow laboratory environmental health and safety policies, keep work surfaces clean and tidy, and correctly use instruments and equipment with corresponding authority.
任职资格:
1、 专科或本科Associate degree or bachelor's degree；
2、 生物、药学或者相关专业Biology, pharmacy or related majors；
3、 具备生物相关知识背景Have biological related knowledge background；
4、 熟练阅读英文文献Proficient in reading English literature；
5、 工作踏实，和团队成员保持有效沟通Work hard and maintain effective communication with team members。