Qa 工作 在 北京

百奥赛图（北京）医药科技股份有限公司

¥15,000 - ¥25,000 /月

该职位来源于猎聘 岗位职责： 1.负责抗体CMC相关的质量管理工作和测试工作； 2.跟进 CDMO 质量协议的审核与签订 3.CMDO 质量事件的调查、管理与批准，偏差，变更以及OOS 4. CDMO主要文件的审核、签署，如MBR，COA，SPEC等 5.年度质量报告回顾 6.跟踪客户质量协议的签订(如IDEAYA，ITEOS，BCG034，BCG017) 任职要求： 生物、医药、免疫等相关专业，3-5年工作经验硕士学历； 2.工作踏实，抗压能力强；

北京同仁堂股份有限公司

¥15,000 - ¥20,000 /月

该职位来源于猎聘 国企正编，直签，双休，包吃包住 工作职责 1、跟进大兴基地战略规划和目标，设定并拆解质量指标，并进行持续追踪以实现目标。 2、质量体系搭建与GMP运维 （1）全面负责公司中药饮片生产质量管理体系建立、落地、更新与持续改进，严格执行《药品管理法》《中药饮片质量管理规范》及GMP相关法规； （2）负责质量SOP、管理制度、验证文件、记录表单的编制、审核、修订与管控，确保体系合规、流程闭环、可追溯； （3）主导年度GMP内审、自查整改、迎检准备工作，配合药监日常检查、飞行检查、专项检查及认证核查； （4）集团系统产品备案：产品执行标准、图稿等审核，确保材料合规。 3、全流程质量管控

Sanofi

Job Information 职位信息 Job title职位名称: QA Specialist QA专员 Location工作地点： Beijing, China 中国北京 % Remote working and % of travel expected 远程办公和出差的概率：N/A Job type工作类型: Full time全职 Site/Unit 区域/事业部：Beijing Site/ M&S China北京工厂/中国制造与供应事业部 About The Job工作职责 Our Team我们的团队： The M&S division encompasses ma

该职位来源于猎聘 职位描述：质量管理体系 QA 岗位职责: 1、负责质量体系文件的发放、回收、复制、借阅、保管和销毁等文件清单、记录清单编制。 2、负责外来文件收集、发放、回收、复制、借阅、保管和销毁等。 3、参与变更、偏差、纠正和预防措施、产品文件的审核、生效。 4、负责退货、客户反馈与投诉的调查、评估与处理。 5、负责供应商的评估、审计，编制并及时更新合格供应商清单、供应商档案。 6、协助完成内审、外部评审工作，监督纠正预防措施的制定和实施。 7、根据工作需要起草、审核相关文件。 8、协助做产品季度风险分析、质量回顾的信息收集、汇总、分析。 9、完成领导安排的其他临时性工作。 任职要求:

AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably. We’re the first software business in the world to ha

该职位来源于猎聘 岗位职责： 1、负责公司纸质文件打印、扫描、装订、编号、归档； 2、建立、维护文件归档台账，登记文件版本、生效状态、存放位置；归档文件借阅登记和文件查找调取 。 3、 电子文件分类整理、命名、文件夹归档，PDF 转换； 4、协助完成历史归档文件整理、盘点，建立历史归档文件详细清单，为后续归档文件新厂转移后分类存储做准备。 5、完成其他上级安排的文件管理岗相关工作。 说明：此岗位如表现出色可优先留用。 任职要求： 1、全职实习生，档案管理、药学、制药工程等相关专业优先，有GMP企业文件归档经验的优先。 2、能够完成重复性文档整理工作；保密意识强，严格遵守公司文件保密管理规定，不

Beijing, China Full time R015475 AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably. We’re the first sof

TELVENT CONTROL SYSTEM (CHINA) CO., LTD

AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably. We’re the first software business in the world to ha

AVEVA

AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably. We’re the first software business in the world to ha

Role profile: An opportunity exists within LSEG for a Lead QA Engineer role within Content & Feeds Technology. ROLE SUMMARY: We are seeking a Lead QA Engineer to join a highly collaborative, cross-functional, software Quality Engineering team responsible for functional testing, performance testi

北京安必奇生物科技有限公司

¥50,000 - ¥80,000 /月

该职位来源于猎聘 岗位职责 1. 建立并维护GLP/GCP/GMP（GCLP）质量体系，覆盖药物物质、药物产品、分析、标签与临床供应 2. 制定并执行内部审计、CRO/CDMO监管与质量事件管理，确保合规 3. 审核批记录与合规文件，支持卫生监管部门检查与申报 4. 推动质量体系持续改进，培训跨职能团队合规意识 任职要求 1. 药学/化学/生物等相关专业硕士以上 2. 5–8年以上制药QA/QC经验，精通cGMP、ICH、FDA/EMA监管要求 3. 在大型药企或头部CRO/CDMO完整做过QA/QC与监管对接 4. 熟悉放行测试方法（HPLC/ELISA/PCR等）与数据完整性，中英文流利

China Asset Management Co., Ltd.

¥35,000 - ¥50,000 /月

该职位来源于猎聘 About AIX AIX is a financial technology company focused on building secure, compliant infrastructure that bridges digital assets and traditional payment networks. Headquartered in Hong Kong, AIX aims to support the region’s position as a global digital-asset and fintech hub, delivering regu

LSEG

Role profile: An opportunity exists within LSEG for a Lead QA Engineer role within Content & Feeds Technology. ROLE SUMMARY: We are seeking a Lead QA Engineer to join a highly collaborative, cross-functional, software Quality Engineering team responsible for functional testing, performance testi

Meitu Inc.

We are looking for native speakers to join our localization team. You will be responsible for reviewing and refining AI-translated content, reviewing in-app copy for cultural appropriateness, and supporting marketing localization — ensuring our products feel natural, culturally appropriate, and nati

该职位来源于猎聘 职责描述： 1、Incoming materials inspection of lens area including lens warehouse and DC; 镜片、包材来料检验 2、Some final product inspection for DC area; 仓库产品最终检验 3、Supplier quality management of lens area including annual materials assessment, supplier auditing, materials validations, daily materials iss

明济生物

¥9,000 - ¥15,000 /月

该职位来源于猎聘 岗位职责： 1.负责体系相关文件的制定与升版、相关质量变更； 2.参与偏差/变更的审核与追踪；制定公司年度培训计划，组织并完成人员培训工作、人员档案管理； 3.制定内部审计计划，组织各部门人员完成内部审计工作并追踪整改； 4.组织参与供应商（原辅包、检验）的现场审计、供应商档案管理。 任职要求： 1.本科及以上学历； 2.5年以上QA工作经验，有上市生物制品核查经验优先，熟练掌握偏差、变更、培训管理要求及管理流程； 3.熟练使用Office办公软件，具备较强的逻辑思维、沟通协调能力及团队协作精神，工作严谨细致，有较强的执行力，确保工作闭环。

IQVIA

Job Overview Assist lead auditors/audit liaisons in conducting, hosting and reporting quality assurance audits by performing specific audit tasks under the direct supervision of more senior QA staff. Essential Functions Assist in conducting quality assurance audits within budget and established time

Job Overview Assist lead auditors/audit liaisons in conducting, hosting and reporting quality assurance audits by performing specific audit tasks under the direct supervision of more senior QA staff. Essential Functions • Assist in conducting quality assurance audits within budget and established ti

Beijing, China Full time R1569370 Job Overview Assist lead auditors/audit liaisons in conducting, hosting and reporting quality assurance audits by performing specific audit tasks under the direct supervision of more senior QA staff. Essential Functions • Assist in conducting quality assurance audit

ApeX Protocol

岗位职责 负责交易平台与自研 L1 链核心链路的质量保障：涵盖撮合、清算、保证金与资金费、下单/撤单、账户与签名、区块持久化、索引与对外接口等模块。 主导重大需求与核心模块的测试策略、方案设计与风险评估，保障业务流程与关键数据的准确性、一致性。 针对高并发、数据一致性、幂等、超时重试、异常恢复、节点崩溃与重启等复杂场景设计测试，验证系统的稳定性与容错能力。 持续开展非指派的系统性风险排查：主动选定模块做深度审查，提出并落地新的测试场景，非等待需求驱动。 建设并持续优化自动化测试体系，推动接入 CI/CD，提升覆盖率、回归效率与交付质量。 参与需求与技术方案评审，负责复杂问题定位、根因分析与质量