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  • 无锡药明生物技术股份有限公司 Wuxi

    无锡市 滨湖区 KEY ACCOUNTIBILITIES: 领导新区DP3厂AIS团队,提供GMP IT 和自动化支持,满足DP业务和DI合规需求 Lead DP3 AIS work stream to provide day to day support in GMP IT and Automation service, meeting business needs and DI compliance. 针对GMP关键设备和生产系统,从技术和合规层面管理计算化系统,提供服务如周期性回顾,数据管理,帐号管理。 Manage computerized system in both technical and compliance aspects, supporting system periodical review, data management, user account management for GMP critical instrument and production skids. 提供PLC自动化专家支持,包括自动清洗,灌装,冻干及包装线。 Provide PLC /a...

  • 无锡药明生物技术股份有限公司 Wuxi

    Job title: Training Associate Director of Training Centre Job responsibilities: 1. The program Associate Director of Training Centre is accountable for developing and implementing an overarching learning services that is aligned to the business needs of the organization being supported. 2. Able to do needs analysis, and build the learning solutions to support the business WX Biologics. 3. Develop and deliver learning programs, such as New Employee Orientation program, as per the annual training ...

  • 广州奈氏力斯生物科技有限公司 Guangzhou

    职位信息 1、通过400客服热线、在线聊天工具、手机客户端、企业官方微博、邮箱、微信公众号等记录客户咨询、投诉内容,按照相应流程引导客户并给予正确及时的反馈处理; 2、受理客户咨询、投诉、建议及意见等,并做好记录。 3、能及时发现咨询客户的需求及意见,并正确及时转交相关部门; 4、具备一定的营养及医药、护理知识;具有良好的沟通表达能力。 任职要求: 1、大学专科以上学历;营养学及医学专业优先考虑; 2、年龄23-35岁,有耐心及责任心,身体健康,能够长期稳定的干好工作; 3、有客服和电话销售经验,有相关工作经验者优先; 4、普通话标准,口齿伶俐;具有较强的沟通能力及服务意识,吃苦耐劳; 5、熟悉计算机办公软件操作; 职能类别:客服专员/助理 关键字:客服专员热线保健品营养品医药护理 微信分享 联系方式 上班地址:广州市天河区珠江新城西侧华明路9-13号东塔1401房 地图 公司信息 奈氏力斯是一家新西兰公司,致力于营养保健品、乳制品、护肤品等家庭健康食品及护理用品的研发、生产及销售,奈氏力斯拥有自己的营养研究中心及制造工厂,产品在全球销售并在于2005年进入中国,合作伙伴包括华润OLE...

  • 武汉中原瑞德生物制品有限责任公司 Wuhan

    Provide legal support for CSL Behring’s Chinese operations and manufacturing activities, including: Review, draft and negotiate all contracts required by the plasma collection centers in China as well as the Wuhan fractionation site in the conduct of its business (except those which are the responsibility of Legal Services) subject to CSL’s Legal Policy, including R&D, plasma collection, fractionation, purchase and sale, distribution, agency, consulting, services, tender consulting, supply a...

  • 武汉中原瑞德生物制品有限责任公司 Wuhan

    生化检测 Microorganism Analyst 岗位职责:Job Description 1. 负责原辅材料/半成品/成品/环境取样,微生物检测和放行; Responsible for sampling of raw materials/excipient/semi-finished products/environment, plus microbiological testing and releasement; 2. 负责产品无菌检测、微生物限度检测及相关验证; Be responsible for product sterility testing, microbial limit testing and related validation; 3. 领用、传代、确认、计数及保存,微生物性状鉴定; The apply/subculture/confirmation/counting/preserve of culture, the ID for the characters of microorganisms; 4. 验证,配合公司验证计划,进行验证检验 Validati...

  • 普罗旺斯欧舒丹贸易有限公司 Shanghai

    Job Responsibility Lead product registration to comply with NMPA and SH-FDA requirements, to ensure the registration on time. Familiar with EU regulation and cosmetic existing usage material list of China, coordinate with Central lab for cosmetic ingredients analysis to comply with NMPA and SH-FDA Regulation for the Application of Administrative Permission for cosmetics Good registration experience about imported non-special cosmetics. Can independently accomplish registration documents for gett...

  • 柏創生活事業有限公司 Kaohsiung

    長期兼職傳單人員 時薪150起&績效抽成獎金另計 派發公司傳單銷售廣告,無經驗可 會有專業人訓練協助 ※平日班:9:00-12:00 ※假日班:13:30-17:30 (時間彈性可溝通) ※薪資:時薪150元(績效抽成獎金另計) 職務類別 : 工讀生 休假制度 : 依公司規定 上班時段 : 依公司規定 年 8 月 23 日 需求人數 : 1至3人 薪資待遇 : 時薪 150 元以上每月薪資行情表我要申訴 工作性質 : 兼職-長期、短期、假日 上班日期 : 隨 時 管理人數 : 不需負擔管理責任 出差說明 : 需出差 外派說明 : 需外派 工作條件 學歷要求 : 無限制 科系要求 : 不拘 工作經驗 : 不拘 技能與求職專長 電腦技能 : 未填寫 必備附件 履歷照片 <職場性格測驗>報告 應徵方式 連絡人 : 潘小姐 Email : 若有意應徵,請直接按「我要應徵」投遞履歷即可。...

  • 北京方生益达科技发展有限公司 Beijing

    北京市 通州区 任职资格: 母语为法语、西班牙语或阿拉伯语; 或多年生活在美、加、澳大利亚或欧洲的华裔; 英语或汉语流利; 流利的外语沟通和独立开发客户能力; 熟练掌握日常函电、外贸流程和标准; 了解基本的国际贸易法规和国际贸易惯例; 对居住地(或主管地区)商超连锁、家用医疗器械行业、运动护具等有利于本公司产品的市场比较熟悉; 具有一定的表达、沟通、协调能力,有较强的开发客户的能力。 岗位职责: 按照公司考核制度、完成业绩指标,并针对给出辅助,建立客户档案、产品档案、出口货物统计台账、不断开拓业务,拓展海外市场; 根据客户下单情况,安排生产,并跟踪订单、交付过程中的交期、质量问题 Qualification: Native speaker of French or Arab; Or Chinese have lived in the United States, Canada, Australia, or Europe for a long period; Good English or Chinese; Fluent in foreign language communication...

  • 佛山市南海祥旺光学电子制品有限公司 Foshan

    职位信息 岗位要求: 1、 3-5年行销媒体运用维护相关经验 2、 3-5年展会概念企划与参展相关经验(有摄影展会经验尤佳) 3、 3-5年年度行销预算制定相关经验 4、 3-5年网站企划管理经验(含网域和社交网站) 5、 3-5年媒体公关关系活动维护经验(含各类新闻稿制定) 6、 3-5年品牌(CIS)形象策略制定/执行经验(含概念) 7、 对市场营销和推广有深入的了解,思路清晰,有一定的策略思考和展现能力,在互联网整合营销推广上具有丰富的经验。 8、 精通中英文 9、 良好的表达沟通能力与具有文化气质的书写能力 10、 精通电脑知识:微软办公室软体, Photo Shop, Illustrator和InDesign等 ,可灵活运用Excel函数,制作报表。如有编辑巨集经验优佳 11、 精通行销/媒体相关用�Z 12、 可接受出差 13、 有摄影器材行业经验者优先 工作职责: 14、 负责产品营销策略制定 15、 掌握行业动态,竞争对手品情况,重点市场环境,制定产品销售方案,挖掘产品卖点。 16、 规划和制定行销材料和素材 17、 产品发布相关活动的策划与支持 18、 开发与产品结合...

  • 上海润诺生物科技有限公司 Shanghai

    岗位职责 ? Lead the bioanalytical method development and non-GLP validation of LC/MS/MS methods, sample analysis, data analysis and modeling, and study protocol and report writing for small and large animal PK, toxicokinetics (TK), PK/PD and biomarker studies. ? Design PK studies, conduct bioanalytical method development, sample analysis, data analysis and PK modeling, and study report writing in support of discovery and IND-enabling PK and TK studies. ? Manage and supervise a small molecule bioanal...

  • 百济神州生物科技有限公司 Beijing

    北京市 昌平区 Job Description The successful candidate will participate in BeiGene’s preclinical programs and use their skill set to accomplish the following responsibilities: ? Design biochemical and cell-based assays through comprehensive literature study ? Develop, optimize and execute assays ? Perform therapeutic target profiling, compound screening and/or support SAR study ? Data analysis and report ? Present scientific data to internal audiences 职位要求: Requirements ? M.S. with biotech/pharma expe...

  • 上海润诺生物科技有限公司 Shanghai

    上海市 浦东新区 岗位职责 ? Design and conduct in vitro (enzyme- and cell-based) and in vivo hepatic and extrahepatic biotransformation studies; Propose metabolite structures and CYP and non CYP metabolic pathways in various biological systems. ? Work proficiently in LC-MS/MS method development, biological sample processing (plasma, bile, urine, feces, plant, tissue), and in detection, identification, structural elucidation and determination of multiple metabolites in various matrices with Q-Trap, Q-Exactiv...

  • 诺华 生物医学研究有限公司 Beijing

    1. Manage collection, processing, documentation, reporting and follow-up of all adverse event reports for all Novartis products from clinical trials, non-interventional studies, Patient Orient-ed Programs, literature, Spontaneous Reports, etc. Transcribe, translate and enter data of all data from source documents into safety systems accurately and consistently with emphasis on timeliness and quality. 2.Manage reporting/submission/distribution of safety reports/updates/information (e.g. SAE, SR, ...

  • 伯乐生命医学产品有限公司 Shanghai

    上海市 杨浦区 概观 Install, configure, upgrade, service, PM and repair instruments which have been sold to customers. Identify and correct problems for bio-rad instruments. Collect instrument quality and service issue and information. Make good relationship between bio-rad and customer. Background knowledge for flow cytometry 职责 Provide commissioning, Pre-installation, Installation, testing and instrument maintenance service for customer. Provide troubleshoot, investigate and resolve technical problems ...

  • 复星凯特生物科技有限公司 Hangzhou

    Key Accountabilities 职责描述: 1, Implements the district business strategy, ensures the achievement of hospitals goals through conducting academic promotion and maintaining networks with customers including hospital presidents, physicians, nurses, pharmacologists, and identifies business opportunities and problem points. 2, Establishes goals in alignment with prescribed business strategies and monitors the progress towards them. 3, Organizes the collection of relevant market access data and potenti...

  • 苏州博腾生物制药有限公司 Suzhou

    job content: Building and leading the virus vector team Responsible for the vector production business Overseeing the research and development efforts in AAV and lentivirus platforms Participating the management meeting, contributing to the overall direction of the gene and cell therapy efforts Providing guidance and training to other employees Representing the department in cross functional teams within the company Representing the company for interactions with customers and other stake holders...

  • 百济神州生物科技有限公司 Beijing

    ? Delivery of clinical start-up component of assigned studies with accountability for time, cost and quality for assigned activities, which include, but not limited to, o Investigator/Site identification, including conduct feasibility activity to identify investigators and conduct site visit to confirm qualification for the required study o Prepare IRB submission o Clinical trial site contract and budget negotiation, if required o Prepare, submit regulatory documents to HGRAC and obtain approval...

  • 苏州博腾生物制药有限公司 Suzhou

    job content: Building and leading the CAR-T team Responsible for the CAR-T CDMO business Overseeing the research and development efforts in immuno-oncology Participating the management meeting, contributing to the overall direction of the gene and cell therapy efforts Providing guidance and training to other employees Representing the department in cross functional teams within the company Representing the company for interactions with customers and other stake holders as needed requirements: 1....

  • 重庆中元生物技术有限公司 Shanghai

    1. Search the most cutting-edge literatures in academic and industrial fields, evaluate the feasibility and apply them to the current platform. 2. Lead molecular biology groups for various projects. Recruit, train and supervise scientists to provide best quality services. 3. Manage project workflow to ensure on time delivery: from initial planning, staffing, to experiment execution, data evaluation and trouble shooting. 4. Communicate results and address issues regularly with colleagues. 5. Deve...

  • 上海百利佳生医药科技有限公司 Shanghai

    POSITION SUMMARY To responsible for timely reporting and processing of respective Serious Adverse Events (SAE), Adverse Event(AE) Serious and non-Serious Adverse Drug Reaction(SADR) and other medically related project information within agreed timeline to Health Authority and other Key Stakeholders. To responsible for document archiving, data tracking communication of respective safety reports in compliance with company’s and relevant regulator’s requirements. JOB FUNCTIONS/RESPONSIBILITYES The ...

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