药明生物
下游生产工程师
岗位职责
JOB RESPONSIBILITY 参加GMP培训,进入车间遵循GMP规范。 Attend GMP training, follow the GMP standards in the manufacturing workshop. 按GMP要求执行蛋白纯化操作,包括溶液配制,层析柱拆装,蛋白纯化工序(层析,病毒灭活,深层过滤,除病毒过滤,超滤,辅料添加和原液分装等操作)。 Perform operation of protein purification according to GMP requirements, including buffer preparation, column packing and unpacking, protein purification (chromatography, viral inactivation, depth filtration, viral filtration, ultrafiltration and diafiltration, formulation and bulk fill, etc.) 起草/升版/审核/废除SOP/MBR等GMP文件的。 Drafting/updating/reviewing/abolishing the GMP documents of SOP/MBR. 按时完成主管安排的其他GMP工作。 Complete other GMP work arranged by supervisor on time.
任职要求
熟练使用office等办公软件。 Highly skilled at office software. 具有较好的沟通能力和理解能力。工作积极向上并具有良好的学习能力。 Have good communication and understanding ability. With an optimistic work attitude and good learning ability. 具有良好的组织能力,强烈的职业道德,并勤于保存数据文档保证数据完整性。 Must be well organized, have a strong work ethic, and be diligent in data documentation for integrity.
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