Are you passionate about driving energy-efficient cooling solutions and helping OEM customers accelerate their sustainability journey? Then join us in our mission to pioneer smarter solutions for moving and transforming water, reducing energy consumption, and enhancing
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
Job Description: As a Supplier Quality Assurance Sr. Analyst at Mars you will lead the global SQA process for MARS, working with suppliers and cross-functional teams (Global Commercial Sourcing, R&D, Manufacturing) to ensure food/material quality systems
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,
Overview Morgan Advanced Materials is a business rich in history and innovation. Founded in the UK in 1856, we have grown into a global organisation with 70 sites in 18 countries. Our model to serve our
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,
Department: CMC Location: Remote with at least 50% travels to site for meetings in Guangzhou, China Employment type: full-time Position Summary: As a key member of Angitia’s leadership team, the ED/VP, CMC Process R&D leads the
Shanghai, China | full time | Job ID: 9282 Your main responsibilities are: Participate in the design and execution of clinical trials of their assigned programs, helping to create the clinical development plan for new compounds,
Shanghai, China | full time | Job ID: 10561 Position Summary: The Safety Strategy Lead China represents a pivotal function in the BioNTech Safety Governance; therefore, the SSL assumes accountability for: an optimal performance of the
Job Description • Translates team’s strategic objectives into operational plans; • provides insight into operational feasibility of proposed strategies. • Drives cross-functional and cross-geographical alignment to strategic plans and goals. • Recognizes and flags internal or
Role Summary: The Development China Clinician is responsible for high quality and timely delivery of one or more interventional clinical trials for R&D. They apply technical excellence in the design of cost-efficient clinical trials to meet
About Us: Structure Therapeutics develops life‐changing medicines for patients using advanced structure‐based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design
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。 · 在
Main Purpose of the job 职务目的： Responsible for supplier quality management, quality control, problem solving, and quality level improvement. 负责供应商质量管理，质量监控，问题解决，质量水平提升 Job Responsibilities工作职责 Participate in the continuous improvement process of the plant, manage the plant quality system
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Company Description Impact the Future. Egis is a leading global organisation in architecture, consulting, construction engineering, operations and mobility services. We partner with clients to design, deliver and operate smarter infrastructure and places that respond to
Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
岗位职责： 技术转移与放大：作为项目研发代表，主导从研发实验室（Lab-scale）到中试车间（Pilot-scale）再到商业化GMP车间（Manufacturing-scale）的技术转移全过程。 抗体药物下游工艺开发的技术骨干，主导从药物发现（DNA to IND）到临床后期（BLA）全周期的下游纯化工艺开发，解决高浓度蛋白聚集、病毒清除验证等复杂技术难题，连接研发（R&D）与生产（GMP）,将实验室规模的纯化路线稳健地转化为商业化生产能力。 下游工艺开发与优化：负责抗体（单抗，双抗，融合蛋白）下游纯化工艺的全流程开发，包括但不限于：深层过滤、亲和层析（Protein A）、离子交换（IEX）、疏水层析（HIC）、混合模式层析、超滤/渗滤（UF/DF）及病毒灭活/去除（低pH孵育、纳滤）。 新平台技术引进：关注行业前沿（如连续工艺、膜层析），评估并引入新技术以提升现有纯化平台的效率和经济性（COGs）。 任职要求： 硕士及以上学历，生物工程、生物化学、化学工程、制药工程或其他相关生命科学专业。 博士学历具有 4年以上或硕士学历具有 8年以上抗体药物下游纯化工艺开发与技术转移经验（特别优秀者可适当放宽年限）。 必须具有至少4个完整项目的工艺开发与技术转移经验，或至少1个完整项目的工艺表征经验，参与过工艺验证的技术支持工作。 精通各类层析纯化技术，对层析介质的化学特性、动态载量及使用寿命有深刻理解。 具备丰富的高浓度蛋白（100 mg/mL）制剂前的超滤工艺开发经验，熟悉跨膜压、剪切力对蛋白质量的影响。 熟练操作AKTA pure/avant/pilot及Unicorn软件，具备一定的编程能力。 熟悉cGMP法规，有在CDMO公司或大型制药公司GMP车间跟产经验者优先。 流利的英文听说读写能力，能够独立撰写技术文件，并在国际协作环境中进行有效沟通。 具备一定的抗压能力和多线程任务处理能力，能够适应项目紧凑的IND申报时间表。 优秀的跨部门沟通能力，能够有效协调研发、生产和质量团队的工作。...
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