职位描述Responsibilities:1.负责文件管理,确保文件控制系统在工厂的有效实施和持续改善。Responsible for Document Control and make sure its effectiveness and continuous improvements2.协助建立新厂的文件管理体系。Assist to develop document management sy ...详情>>
职位描述岗位职责:协助上级建立验证文件体系,确保其符合法规及百济神州的质量要求Assist managerfor establishing validation documentation system and make itconform to the regulations and the BeiGene Global quality requirements协助上级搭建人才发展梯队,发展团队 ...详情>>
职位描述岗位职责:做为LMS系统负责人,管理GMP相关培训;As the systemowner of LMS and responsible for all related GMP training.组织新员工的GMP相关培训; New employee'srelated GMP training.负责人员培训记录及档案的管理;Responsiblefor personnel training ...详情>>
职位描述岗位职责:- Set up maintenance SOPsand carry out regular maintenance ofassigned equipment, such as filling and packagine equipment, clean utilities. 为指定的设备如灌装、包装设备,洁净设施建立维护保养SOP,并执行定期的维护保养;- Perform th ...详情>>
职位描述岗位职责:1、负责文件管理,确保文件控制系统在工厂的有效实施和持续改善;Responsible for Document Control and make sure its effectiveness and continuous improve.2、负责GMP文件的归档登记和保存;Responsible for all document related GMP enclosed and ...详情>>
职位描述职位要求:1、本科或以上学历,药学,生物学或化学专业;Bachelor or above degree in Pharmacy, Biology, Chemistry, etc;2、医药行业2年以上药物分析工作经验; 3 years working experience in pharmaceutical analysis; ?3、熟悉中国药典、美国药典、欧洲药典及GMP/cGMP/欧盟G ...详情>>