岗位职责： Lead the coordination and communication among Zhuhai PD department； Align with PM, RA, QA, QC and relevant departments to move projects forward； Communication with the external vendor for outsourcing projects； Communication with the GTD team
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs
About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Purpose: The Associate Director, Scientific Development supports and leads assigned customer- and commercial-focused strategic development engagements that accelerate business growth, customer impact, and coordinated scientific solutioning. This role connects
About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China. For this green field operation, we’re enhancing our legacy of excellence and build on
About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China. For this green field operation, we’re enhancing our legacy of excellence and build on
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Shanghai, China | full time | Job ID: 11516 Your contribution: Represent External QC Network at CMOs (predominantly located in China) ensuring QC and GMP requirements of BioNTech are considered Represent external/global QC in multidisciplinary project
岗位职责： · 领导并建设一支高绩效的质谱表征团队，持续推进表征分析平台能力建设，包括仪器、分析方法及团队成员技术能力的系统提升。 · 负责从早期研究到后期开发及 BLA 申报阶段的产品表征策略，支持 BsAbs和ADC 项目在以下方面的工作：可开发性评估；IND / BLA 阶段的产品表征研究；工艺开发与优化；可比性研究；关键质量属性（CQA）评估；复杂问题的分析与技术支持。 · 以中英文撰写、审核技术报告及注册申报相关文件（IND、BLA），确保所有表征数据满足注册申报的法规要求。 · 与 CMC、法规事务（RA）、项目管理（PM）及全球团队紧密合作，高效推进项目进展。 任职要求： · 教育背景：蛋白质组学、生物化学、分析化学或相关专业硕士或博士学位。 · 工作经验：6 年及以上治疗性抗体（BsAbs/ADC）表征分析相关的扎实经验；3 年及以上蛋白质组学实操经验；3 年及以上技术团队管理经验。 · 语言能力：具备良好的中英文口语沟通能力，能够流利进行专业交流与技术写作。 · 在治疗性抗体（BsAbs/ADC）的表征分析方面具备系统的专业能力，包括但不限于：蛋白结构表征；宿主细胞蛋白（HCP）的鉴定与定量；翻译后修饰（PTM）及序列变异分析；双抗、ADC 及其连接子-载荷相关杂质或变体的深入表征与解析。 · 熟悉多种正交分析技术，包括但不限于 HPLC、CE、iCIEF、ELISA、BLI/SPR、CD、DSF/DSC、DLS、AUC 等。 · 具备优秀的问题分析与解决能力，能够独立排查并解决分析技术难题。 ·
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Shanghai, China | full time | Job ID: 11325 Position Summary: The main responsibility of this role is to provide project overarching analytical support within the China organization and serve as a local interface for all
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines
Typical Accountabilities Responsible for Quality Supplier Management including but not limited to: Annual Assessments; Quality Agreements; trending and reporting of data; assessing, reviewing and improving quality systems at Suppliers; attendance at Quality and Business Review Meetings.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsStanding for full shift Job Description Job Title: Sr. QC Technician Reports To: Quality Manager Group/Division: China Operation Career Band: B3 Job Track: Associate/Professional/Management Position Location: CMC factory, Guangzhou, PRC Number of Direct
DNV-Area China South is part of the Maritime Region Greater China and consists of more than 100 employees in 4 major locations. Services delivered are related to ship classification of vessels and offshore units as well
岗位职责： 执行ADC与 BsAbs 项目的分析方法的开发、优化、确认、转移及相关问题的排查工作。 执行从早期研究阶段至临床阶段的样品检测工作，按要求完成实验、记录、数据整理。 参与撰写中英文SOP、分析方法开发及确认报告，以及其他相关技术文件。 与 CMC 团队及相关职能团队保持良好沟通与协作，支持项目研发工作的顺利推进。 任职要求： 教育背景：生物化学、分析化学或相关专业硕士或应届毕业博士学位。 工作经验：4年及以上治疗性抗体（ADC/BsAbs）分析开发相关实操经验。 语言能力：具备使用中英文撰写技术报告的能力；具备英语口语交流能力者优先。 对基于色谱的分析技术原理具备扎实理解，并具备相应的实操经验，包括但不限于：分子排阻色谱（SEC）、反相色谱（RP）、疏水相互作用色谱（HIC）、离子交换色谱（IEX）、亲水相互作用色谱（HILIC）、亲和色谱（Affinity Chromatography）等。 熟练操作并维护不同厂商的 HPLC / UPLC 系统的经验，包括 Agilent、Thermo 及 Waters 等主流平台。 具备 IND 申报支持经验（参与 ≥1 个 IND 项目）。 具备良好的问题分析与排查能力，自我驱动，具有良好的团队合作意识，能够积极支持团队工作。...
岗位职责： 执行ADC与 BsAbs 项目的分析方法的开发、优化、确认、转移及相关问题的排查工作。 执行从早期研究阶段至临床阶段的样品检测工作，按要求完成实验、记录、数据整理。 参与撰写中英文SOP、分析方法开发及确认报告，以及其他相关技术文件。 与 CMC 团队及相关职能团队保持良好沟通与协作，支持项目研发工作的顺利推进。 任职要求: 教育背景：生物化学、分析化学或相关专业硕士或应届毕业博士学位。 工作经验：4 年及以上治疗性抗体（ ADC /BsAbs）分析开发相关实操经验。 语言能力：具备使用中英文撰写技术报告的能力；具备英语口语交流能力者优先。 对基于电泳的分析技术原理具备扎实理解，并具备相应的实操经验，包括但不限于：毛细管SDS电泳（CE62SDS）、毛细管等电聚焦（cIEF / iCIEF）、毛细管区带电泳（CZE）、SDS62PAGE、二维凝胶电泳（2D62gel）等。 熟练操作并维护电泳分析仪器的经验，包括 PA800、iCE280、Maurice、Biophase 8800 等平台。 具备 IND 申报支持经验（参与 ≥1 个 IND 项目）。 具备良好的问题分析与排查能力，自我驱动，具有良好的团队合作意识，能够积极支持团队工作。...