杭州招聘

? QC document management. Assist in test records collection and documentation.
QC文件管理。协助进行检验记录的收集整理。
? Reagents and reference materials management.
负责试剂及参考品/标准品材料的管理。
? Assist in sample management, consumables management etc.
协助进行样品管理、常耗品管理等。
? Assist to problem solving, failure investigations and improving lab systems associated with laboratory work such as OOS/DR investigation.
协助实验室相关的问题解决、失败事件的调查和实验系统的提高，如OOS调查、偏差调查。
? Maintain GMP compliance and documentation.
确保符合GMP和文件要求。
? Maintain compliance with legal regulations on occupational safety and health, particularly with regard to hazardous materials.
确保遵守有关职业安全和健康的法例法规要求，尤其是毒害品方面的要求。
? Comply with laboratory policies and procedures.
遵守实验室规章制度。

浙江天元生物药业有限公司 诚聘