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Reporting to Senior MEP Manager, this role will be responsible for project management of capital works projects in. Support the team in managing the project team comprising of external consultants, contracts and suppliers as well as internal cross divisional groups in design stage through to completion, handover to stakeholders and defects rectification.
As the Analytical Chemistry Manager you will play a pivotal role in ensuring the quality and reliability of our products for clients in the personal care, pharmaceutical, and nutrition health industries. You will assist the Analytical Director in managing and enhancing team operations, oversee analytical method development and verification, and ensure compliance with industry standards.
负责工厂的大分子生物药商业化生产的质量全面管理。
作为生产制造副总全面管理下属生产、质量等多业务板块,提升公司GMP体系符合FDA/EUGMP标准。推动无菌制剂临床样品生产以及后期商业化生产进程。
ADC Production Head
This job is take charge of clinical Quality Management System (cQMS) building up and maintenance to ensure all clinical development activities' quality in line with the company's strategy, ICH-GCP and international regulations.
This role is required to establish Quality Management System strategy from planning to execution at Align China site to fulfill requirements of appropriate domestic and international quality system regulations and standards. is responsible for working seamlessly with site quality head and functional teams to ensure QMS at each site is working in effective way and harmonizing with Align global QMS plan as well.
Fantastic opportunity to join a growing chemical businessFast Growth Business Status
we are hiring a facade manager
Taking over previous international managementOverseeing and ensuring all operation excellence
The role is responsible for NPI and NPD and/or their implementation in production, value engineering to MP (Mass Production), automation,advanced solutions and process improvement, supporting production and customers'needs. It reports into global engineering head and local general manager.
作为公司芯片部门一把手,负责数模混合+射频芯片架构设计,并搭建团队完成开发工作。
全面负责工厂的生产管理,不限于车间生产,工艺,设备,EHS的管理。
负责公司药物质量研究工作及质量管理体系的建立和发展。
我们的客户是快消食品领域一家以技术创新及国际化为战略导向,集研发、生产、销售、技术服务为一体的综合服务提供商,全球供应链体系,布局海外市场。现因业务发展需要,招聘一名工厂总经理。
公司在泰州投资新建工厂,2024年全面投产,工厂即将进入设备调试以及试车阶段。需要一位厂长全面管理小试中试到量产的全流程。
负责推动符合FDA标准的新建车间的建设,提升与完善质量体系至符合cGMP标准并推动后期的FDA官方审计
一年内,完成MAH-CMO及MAH-CDMO管理体系建立,并在企业落地实施一年内,结合战略部署,帮助至少2个产品项目技术转移落地。一年内,推进集团内重点项目开展,至少再项目关键节点赋能指导4次其他工作:结合领导安排,协助完成质量板块相关工作。
我们的客户是由一群具有使命感的清华博士联合成立,致力于解决制药行业上游研发设备的技术瓶颈。目前已有三款产品实现商业化,进入规模量产阶段。伴随企业成长亟需了解GMP和FDA的质量专家,来建立质量管理体系,协助企业走向国际化市场。
负责CMC团队的建立、完善和管理;制定原料药和制剂的开发策略和生产计划;指导解决新药工艺开发过程中的关键技术问题;负责管理外包研发生产服务供应商;负责与监管部门在CMC方面的沟通和交流;配合临床部门开展临床试验,提供药学方面的支持;配合注册部们完成各项目IND/NDA申报资料的撰写、审查,配合完成现场核查及注册申报。
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