上海今日更新的139个qa职位机会
个职位
· 页 1 / 7Job Description: Essential Job Functions: • Participate in software development projects by writing, testing, and debugging code, under the guidance of more experienced team members. • Collaborate with team members to achieve project objectives and meet deadlines. • Contribute to the documentation o
Job Description: Essential Job Functions: Participate in software development projects by writing, testing, and debugging code, under the guidance of more experienced team members. Collaborate with team members to achieve project objectives and meet deadlines. Contribute to the documentation of soft
In this role, you will have the opportunity to: Manage GSP-related policy and compliance affairs for Cytiva medical devices. (i.e. Compliance with Shanghai MPA and Pudong Market Bureau requirements, Ad Promo Material filing as needed) Support the line manager in delivering successful localization pr
In This Role, You Will Have The Opportunity To Manage GSP-related policy and compliance affairs for Cytiva medical devices. (i.e. Compliance with Shanghai MPA and Pudong Market Bureau requirements, Ad Promo Material filing as needed) Support the line manager in delivering successful localization pro
In this role, you will have the opportunity to: Manage GSP-related policy and compliance affairs for Cytiva medical devices. (i.e. Compliance with Shanghai MPA and Pudong Market Bureau requirements, Ad Promo Material filing as needed) Support the line manager in delivering successful localization pr
In this role, you will have the opportunity to: Manage GSP-related policy and compliance affairs for Cytiva medical devices. (i.e. Compliance with Shanghai MPA and Pudong Market Bureau requirements, Ad Promo Material filing as needed) Support the line manager in delivering successful localization pr
该职位来源于猎聘 工作职责： 1、负责官方、客户审计准备工作及CAPA回复； 2、监督生产过程、实验室活动、仓库和公用系统（水、空调、氮气、压缩空气）符合SOP及cGMP要求； 3、确保完成内部审计和自检； 4、负责物料供应商、合约服务商的管理； 5、负责质量保证部的文档管理工作； 6、负责批准仓库和公用系统（水、空调、氮气、压缩空气），设备计量相关的操作规程。 任职条件： 1、本科及以上学历，医药或化工类相关专业； 2、具有5年以上制药企业质量管理经验，有产品放行、验证、质量文件体系、现场符合性等相关工作经验； 3、熟悉GMP、ICHQ7相关法规； 4、良好英语阅读和沟通表达能力； 5、有接
该职位来源于猎聘 职责描述： 1.负责药学研究原始记录（实验记录、仪器使用记录）等进行检查； 2.负责审核方法学验证方案和报告；稳定性考察方案和报告； 3.负责审核中试工艺规程、批生产记录、质量标准（或分析方法）； 4.负责跟踪药学项目计划的实施情况，按照研发流程对关键研发节点评估、讨论会议的组织； 5.配合完善研发中心各部门工作衔接的规范性； 6.配合完善研发质量体系； 7.其他部门内部工作。 岗位要求： 1、药学，制药等相关专业本科以上学历 2、熟悉质量管理体系 3、熟悉CFDA相关药物研发指导原则及法规要求 4、熟悉研发流程、具有药品研发项目管理经验优先 任职要求：
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the
该职位来源于猎聘 QA Manager Reporting locally to：QARA Director Objectives and scope of the job Tasks / Activities Manage the daily maintenance, internal audit and continuous improvement of ISO13485 QMS for Marketing Unit. Lead the 0-1 establishment and implementation of the GMP for the China factory. Establ
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the
该职位来源于猎聘 RESPONSIBILITIES 职责 Leading QA and verification activities of new products in R&D phase: 主导产品在研发阶段产品质量保证以及验证方面的活动 Work with internal R&D, quality team and ODM/OEM vendors to: 和公司内部研发和质量团队以及ODM/OEM供应商一起: Review the FFU and DFM of the product design from ODM/OEM suppliers or in-house.
该职位来源于猎聘 岗位职责： 1、质量文件与体系管理 负责质量体系文件（SMP、SOP等）的分发、修订与控制，确保文件现行有效、受控可溯；根据业务需求起草和优化体系文件。 2、服务商及研发沟通 负责沟通服务商及研发人员，开展与研发实际需求相适应的验证/确认、校验校准管理工作。 3、研发过程合规管理 负责研发试验记录的日常检查，确保实验室数据符合及时性、完整性和可追溯性要求；跟踪与项目相关的偏差、变更、CAPA等质量事件，及时汇报进度并推动闭环。 4、CDMO/CRO文件与档案管理 负责外来文件（CDMO/CRO等）的管理，按法规要求建立并维护产品档案。 5、产品放行审核与数据跟踪 收集并审核产
Onsite Shanghai, Shanghai, China Full time R81378 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing
该职位来源于猎聘 1. 搭建、修订、维护临床质量SOP与管理制度，建立适配公司规模的临床质量体系，跟进法规更新，组织内部GCP培训。 2. 制定QA稽查计划，独立开展临床试验项目全流程稽查（立项、伦理、中心启动、入组、结题归档），监控CRO工作质量。 3. 撰写稽查报告，跟踪缺陷整改闭环；管理偏差、方案违背，建立质量风险台账，识别并防控临床合规与数据风险。 4. 负责药监核查、伦理审计、第三方审计的迎检准备，统筹临床质量档案管理。 5. 定期输出质量总结报告，对接临床、注册、研发等团队，落实质量要求。 任职要求 1. 本科及以上，药学、临床医学、生物、预防医学等相关专业。 2. 3年及以上药物
MedtronicCareers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the
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, allowing you to thrive both personally and professionally. This is how
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, allowing you to thrive both personally and professionally. This is how
明慧医药（上海）有限公司该职位来源于猎聘 岗位职责： 1、 产品生产工艺、技术转移、验证/确认等文件合规性审核； 2、委外生产和委外检验交付文件的合规性审核； 3、参与服务商/供应商的现场审计； 4、 细胞库、中间产品、产品的放行审核； 5、协调所对接CMO相关的质量事件的调查处理、CAPA审核与跟踪（偏差、变更、投诉、退货、异常、不良反应及召回事件等；） 6、审核CMO的年度产品质量回顾及持续稳定性考察数据，监控产品质量趋势； 7、关键批次的现场驻厂及问题的跟踪落实； 8、 参与注册申报资料审核（IND/BLA)。 任职要求： 1、教育背景：药学或生物工程相关专业，本科以上学历； 2、岗位经验：5年以上商业化药企生
RocheAt 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, allowing you to thrive both personally and professionally. This is how
GetingeWith 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. To make a true difference for our customers – and to save more lives, we need
GetingeWith 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. To make a true difference for our customers – and to save more lives, we need
GetingeWith 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. To make a true difference for our customers – and to save more lives, we need
QMS Process maintenance & improvement 质量体系流程维护和优化 Drive product quality improvement and cost of quality improvement 推动产品质量改进和质量成本优化 Distributor management & audit 经销商管理和审核 Document control and quality training management 文件控制及质量培训管理 Advertising and promotional material review and submission
Job Summary The role has oversight and governance of quality management systems, quality assurance and quality control for the manufacturing plants in APAC, and supports the local 3PM team for quality related assessments and service arrangements. Responsible for administering and resourcing the prog
Crimson Education is the world’s leading college admissions consulting firm, with over 1,490 Ivy League offers and 2,410 to the US Top 15. We help ambitious students gain admission to the world’s top universities through expert-led guidance and proven, data-driven strategies. Crimson students are 7x
Lincoln ElectricLincoln Electric is a high-performance industrial machinery and technology leader who helps customers manufacture and maintain vital equipment and infrastructure. Lincoln Electric’s innovative solutions enable higher quality and productivity across a variety of processes including welding, cutting,
昆明霸王茶姬餐饮管理有限公司职位来源于实习僧。 职责描述： 1、支撑供质量中心应链QA上新组业务信息汇总和收集； 2、需要汇总和收集供应链上新组从各个端得到的产品上新信息，对涉及上新的新增供应商审核需求（准入、中试、跟产），SQA差旅行程，报告，进度等情况进行统计和输出； 任职要求： 1、本科及以上在校生 2、数据分析专业优先 3、满足产品快速上新需求，整合研发中心、供应链中心、质量中心各端口信息，统计SQA出差情况，审核情况，报告完成情况，收集整合相关信息、跟进上新时间进度，有项目管理经验优先。 职位薪资： 150-180/天 想要了解更多，可以访问公司官网： http://www.chagee.com
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