Cmc Jobs In China - 25 Job Positions Available

Job Description Job Responsibilities Leadership and Team Management: Manage a team within China RA CMC, including performance management, training, workload oversight, and support for a healthy work-life balance. Ensure team activities are delivered effectively, efficiently, and in

Work ScheduleFirst Shift (Days) Environmental ConditionsStanding for full shift Job Description Job Title: Leader QC Technician Reports To: Quality Manager Group/Division: China Operation Career Band: Band IV Position Location: CMC factory, Guangzhou, PRC Position Summary: (1-2 sentences)

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier,

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。...

Job Description Support of the company Portfolio (85%) Lead cross-functional project teams in the strategy planning, execution, and delivery of China new product development projects. Develop project milestones and deliverables; prepare reports that summarize key progress

About us BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Typical Accountabilities 主要职责 Qualification and Validation 确认和验证 To update SVMP and ensure the visibility of validation plan execution status across the site; 更新工厂验证主计划，确保其执行状态的可见性； To coordinate with the site QSR implementation; 协调工厂QSR的实施 To give the training on

Shanghai, China | full time | Job ID: 11750 About the Role: As Director External Supply Organization, you will play a pivotal role in driving BioNTech’s external manufacturing strategy, ensuring seamless collaboration between our contract development

珠海，中国 | 全职 | Job ID: 11766 About the role: 负责领导理化分析团队及平台建设，支持BsAbs项目从早期开发到商业化申报阶段的分析开发工作，涵盖关键质量属性（CQA）分析方法开发、验证与转移，以及复杂分析问题解决。负责技术报告和注册申报文件的撰写与审核，确保数据符合科学和法规要求。 Lead the Physicochemical Analysis team and BsAb analytical platform development, supporting analytical development activities for ADCs from early development through regulatory submission. Oversee CQA method