Job Description The Global Quality - Large Molecule Analytical Sciences (GQ-LMAS) team leads the global analytical technical oversight of late-stage pipeline programs through commercialization and launch as well as product lifecycle management support for Large Molecules (Vaccines
Job Description SummaryAs related customer equipment, faciliaties or infrastructure projects: responsible for project delivery, profit & loss accountability, and customer satisfaction through management of project related activities and resources. Impacts departmental operations and responsible for planning/execution. The
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
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology
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,
Role Overview The Service Design Team has the opportunity of early engagement within product development and therefore to directly impact the experience of customers regarding the effectiveness of the Dyson Service Proposition. We have a responsibility
Role Overview The Service Design Team has the opportunity of early engagement within product development and therefore to directly impact the experience of customers regarding the effectiveness of the Dyson Service Proposition. We have a responsibility
Work ScheduleStandard (Mon-Fri) Environmental ConditionsSome degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials Job Description Position
Company Description Since its spin-off in September 2025 AUMOVIO continues the business of the former Continental group sector Automotive as an independent company. The technology and electronics company offers a wide-ranging portfolio that makes mobility safe,
We are Reckitt Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world.
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we
Typical Accountabilities (per AZ framework and regulatory expectations): Acting as the quality Approval / Decision maker for the GxP relevant procedure in Astrazeneca Distribution Facility. Ensure the compliance with internal Astrazeneca requirement and also relevant market
Job ID: 41721 | Location: Jianping, Liaoning, China | Work Model: Onsite Responsibilities 生产管理 Production Management 根据生产计划管理生产流程：根据客户服务人员下发的订单，在保证合理库存的情况下，制定生产计划；负责组织、协调、调配各种生产性资源进行生产，如人员、物料、生产设备等，及时交货，并保证产品的质量和数量。 Manage production process with alignment to production planning: Based on the orders issued by customer service desk, develop a production
Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing
南通，中国; 珠海，中国 | 全职 | Job ID: 11669 About the role: 百欧恩泰（珠海） MAH质量保证（QA）负责人是一个领导岗位，负责监管本公司及其CDMO（合同开发与生产组织）的所有质量保证活动。该负责人将确保生物制品的生产、检测、放行及分销环节均符合监管要求、行业标准以及BioNTech内部的各项政策、标准和标准操作规程（SOP）。此外，该负责人将建立和提升百欧恩泰（珠海） MAH质量管理体系（QMS）包括监管CDMO相关活动，对CDMO实施质量监督，推动持续改进举措，与跨职能团队协作，并确保产品质量与患者安全达到高标准。该岗位负责产品放行给临床试验和商业化市场 The QA Head for BioNTech-Zhuhai MAH is a leadership role responsible for the quality assurance of the drug products manufactured by BioNTech
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
南通，中国 | 全职 | Job ID: 11655 About the role: 该岗位将全面负责公司原液生产车间（包括上游细胞培养和下游纯化）的运营管理、团队建设和战略规划。需要确保所有生产活动严格遵循cGMP法规、公司SOP和质量标准，安全、高效地完成临床及商业化阶段的生产任务，并持续推动生产工艺的优化和创新。 This role will oversee operational management, team development, and strategic planning for the companys drug substance production facilities (including upstream cell culture and downstream purification process).
Interested in a career that matters? Responsibilities Responsible for daily technical management of utility systems to ensure stable system operation and continuous supply to production. Understand the control logic, interlock conditions, alarm settings, and key control parameters
Location:Datong, Shanxi, China Job ID: R0117221 Date Posted:2026-01-30 Company Name:HITACHI ENERGY DATONG TRACTION TRANSFORMERS CO., LTD. Profession (Job Category):Engineering & Science Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy Transformer Business Unit in
Company Description The present and future of Audemars Piguet are built on the invaluable contributions of all our talents. Inspired by the wealth of our past, we are excited about the endless possibilities that our future