Batch Release Jobs In China - 14 Job Positions Available

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring

With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people.

Typical Accountabilities Specific Responsibilities/Tasks Establishment and maintenance of Quality Management System (A Certificate) of ADC products Being responsible for establishing and maintaining the Quality Management System of ADC products that comply with the requirements of the

Job title: Quality Manager MES (IFB) Job type: Permanent, Full time 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

Community and Community Operations社区与社群运营（海外方向） Hangzhou Experienced Full-time Responsibilities Develop content release rhythm and complete content channel construction through mainstream overseas platforms (Discord, Reddit, X/Twitter, TikTok, Instagram, YouTube);-Identifying and developing early creators: finding people who are passionate about

Purpose & Overall Relevance for the Organization: This role Senior Manager - AI Architect is to lead the architecture design, technical governance, and solution blueprinting of enterprise AI and Generative AI solutions. This role will act

Job Description EXTERNAL QUALITY ASSURANCE -Senior Specialist Qualified Person (QP) China The Position The Product Quality Manager (PQM) Senior Specialist is responsible for ensuring that all Company products managed by External Quality Assurance (EQA) are manufactured,

Job Summary Are you ready to take your skills to the next level and make a real impact? IFF is a global leader in flavors, fragrances, food ingredients and health & biosciences, we deliver sustainable innovations

Company Description Do you want beneficial technologies being shaped by your ideas? Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and building technology - with us, you will have the chance

Be part of something bigger! As the world and the way people live is changing, we at Bekaert believe it’s our responsibility to contribute to finding new solutions for the future. With a 140+ year old

Job Description 岗位概述： 负责兽用疫苗产品在生产过程和放行前的质量检验与实验室管理，确保检验结果准确、合规并符合公司及监管机构的质量标准。作为QC团队的核心执行者，需协同生产、研发等部门，推动检验方法的优化与实验室持续改进。 主要职责： 协助QC经理建立和完善质量控制制度、检测流程，推动质量体系持续改进； 主导中国兽药典检测方法、兽药GMP等法规要求的落地执行； 监督并参与病毒含量、外源病毒、细胞库建立、菌毒种扩繁等工作； 协助QC经理审核检测记录、分析报告、分析方法验证、设备验证等放行文件； 分析检验趋势数据，提出质量改进建议，参与实验室流程优化与成本控制项目； 组织和跟进偏差、CAPA（纠正与预防措施）、变更控制，推动根本原因分析并实施改进措施； 配合GMP等监管检查与客户审计，准备审计资料并组织回复； 与研发、生产及公司其他工厂保持沟通，参与方法验证、方法转移、稳定性试验及质量问题解决。 任职要求： 学历专业：本科及以上学历，微生物学、生物制药、药学、兽医、生物技术等相关专业。 工作经验：5年以上动物生物疫苗行业QC工作经验，具备生物疫苗批检验、稳定性研究及方法学验证经验者优先。 专业能力：熟悉中国兽药典检测方法、兽药GMP等相关法规与标准；熟悉细胞培养、病毒培养等生物学方法及质控技术，能独立解决复杂的质量问题。 核心素养：具备较强的问题解决能力、数据分析能力和项目推进能力，能独立开展组织协调与跨部门沟通能力；数据敏感度高，逻辑严谨，责任心强，能承受一定工作压力；英语流利者优先。 Required Skills: Adaptability, Analytical Instrumentation, Analytical Method Development, Decision Making, Detail-Oriented, Forensic Chemistry, Good Manufacturing Practices (GMP), Laboratory