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多肽主管(J13220)

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Onsite

多肽主管(J13220)

上海凯莱英生物技术有限公司

多肽主管(J13220)

2 months ago

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Important information


Contract type:

Permanent

Location:

Tianjin, China

Work mode:

Onsite

Published on:

16 August 2026

What they need


该职位来源于猎聘 职责描述: 1.多肽类创新药工艺设计和工艺优化。根据项目所处阶段,提供所需的研究内容和原料药。解决工艺开发和质量相关的技术问题。 2.熟悉创新药CMC阶段项目研发流程和研究尺度,包括IND阶段,临床阶段,NDA阶段; 3.在公司SOP体系和质量体系下进行原料药的GMP生产 4.撰写CMC相关申报研究资料,满足新药注册要求。 5.根据客户的需求撰写技术proposal和报价。项目执行阶段负责与客户技术沟通和关系维护。 6.组建和领导合成工艺研发团队,制定计划,跨部门协调资源推进项目。 7.对团队进行技术培训,提升团队业务水平。建立优化所负责团队组织架构。 8.负责所属团队的实验室管理和安全运行。 任职要求: 1、博士工作2年以上,或者硕士工作5年以上; 2、 有机化学,药物化学相关专业; 3、 具备创新药CMC经验和GMP生产经验,多肽类创新药经验优先考虑; 4、 有团队管理经验; 5、 有国外客户沟通经验的优先考虑

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