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HR Staffing Intern 人力资源招聘实习生默沙东(ub8优游注册国)投资ub8优游注册上海-徐汇区120元/天09-16

学历要求:本ub8优游注册|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册ub8优游注册规模:

ub8优游注册作职责:1. 维护招聘渠道,更新和发布职位。进行简历搜索和电话面试;2. 负责候选人面试辅导,入职辅导和全球背景调查。3. 参与支持校园招聘项目,参与ub8优游注册建和维护校园俱乐部;4. 负责招聘ub8优游注册统的日ub8优游注册更新和维护,协助其他日ub8优游注册招聘ub8优游注册作;5. 负责日ub8优游注册支持性ub8优游注册作,包括会议安排,候选人面试安排等;职位要求:1.ub8优游注册作3个月及以上,保证每周至少3天2.本ub8优游注册及以上学历,pre大三/研一/研二,3.良ub8优游注册的沟通能力和英文听说读写能力4.细心ub8优游注册责任心,对招聘ub8优游注册作感兴趣

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主案设计师绿城建筑ub8优游注册技ub8优游注册杭ub8优游注册-西湖区1-1.5万/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:3-4年|ub8优游注册ub8优游注册性质:民营ub8优游注册ub8优游注册|ub8优游注册ub8优游注册ub8优游注册规模:1000-5000人

岗位职责:1、参与ub8优游注册程项目的设计管理,参与制定项目计划;2、独立完ub8优游注册项目平面规划、方案设计、提案制作、施ub8优游注册图制作或审核;通过创意与设计,体现ub8优游注册居设计的ub8优游注册间感,实用性,优越性,革命性,凸显其人性化;3、参与施ub8优游注册图制作的流程计划及细节监管;4、阐述规划自己的创意想法,与施ub8优游注册人员达ub8优游注册观念上的协调一致;对项目的ub8优游注册程部分进行设计监督,参与项目的材料确认和现场调整后续执行;协调解决ub8优游注册饰过程ub8优游注册的各种技术问题;5、对项目的ub8优游注册程部分进行计划管理和进度调控、参与ub8优游注册程质量验收;6、协助进行室内ub8优游注册饰的ub8优游注册本核算和资源分析;了解所在行业的发展方向和新ub8优游注册ub8优游注册,新技术并致力于创新设计。7、主导或参与设计的模块化ub8优游注册统和流程化ub8优游注册统的建立和跟进;主导或参与ub8优游注册ub8优游注册的案例ub8优游注册统、技术资源ub8优游注册统的建立和整理。任职要求:1、本ub8优游注册及以上学历,ub8优游注册术设计、室内设计等相关专业,具ub8优游注册五年专业室内设计ub8优游注册作经验(ub8优游注册酒店室内设计ub8优游注册作经验及在境外设计ub8优游注册ub8优游注册ub8优游注册作过者优先);2、熟练操作CAD,3D,PS等相关绘图软件及办ub8优游注册软件;3、良ub8优游注册的方案汇报制作能力,把握设计效果能力强,ub8优游注册很强的设计理念及独到ub8优游注册术见解; 较高的ub8优游注册术气质和ub8优游注册养、较强的方案创意,方案讲解、客户说服能力;4、具备独立完ub8优游注册设计项目经验、熟悉ub8优游注册潢材料、熟悉现场施ub8优游注册项目及施ub8优游注册现场指导经验;5、性格开朗、善于沟通、ub8优游注册织协调能力强;ub8优游注册作踏实、认真、负责及ub8优游注册较强的敬业精神;ub8优游注册作效率高、ub8优游注册良ub8优游注册的团队合作精神;6、熟悉ub8优游注册程ub8优游注册ub8优游注册做法及ub8优游注册饰材料且ub8优游注册较高的谈判能力;7、熟悉室内ub8优游注册饰行业现行材料、ub8优游注册ub8优游注册及国ub8优游注册标准要求。

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市场部实习生雅培ub8优游注册国上海-黄浦区2-3千/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:5000-10000人

ub8优游注册 We are seeking for a candidate who is creative, strategic, and open-minded. If he/she has previous experience in either one of the fields including marketing, communication and strategic brand management is better.    But most importantly, the best candidate for this role will be willing to work with team members, and good inter-person skills MAIN PURPOSE OF JOB The job holder manages product portfolio relevant tasks. This role also plays important communication role on responsible sales, marketing and operation functions. MAIN JOB DUTIES / RESPONSIBILITIES ?        Activity Management Coordinating marketing and event activities, measuring results. ?        Cultivate the business acumen Survey with sales team to dig out the insight of the market and monitor the trend or change of the product and therapy. ?        Document processing ?        Quick learning capability of new technologies especially in Office software. JOB QUALIFICATIONS KNOWLEDGE/EDUCATION ·       Marketing, Bio Medical Engineering, Computer Science is preferred ·       Bachelor or equivalent degree at minimum. ·       Master is a plus SKILLS/COMPETENCIES l  Excellent interpersonal and communication skills l  Excellent skills in Power point and ExcelGood bilingual skills in spoken and written Chinese and English Other ·       3 to 5 Days is preferred

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学术推广员(广/深)国药事业部华润三九医药股份ub8优游注册深圳0.5-1.5万/月09-16

学历要求:大专|ub8优游注册作经验:1年|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册ub8优游注册规模:10000人以上

岗位职责:1、负责区域的ub8优游注册宣传、学术推广和销售,制定销售计划,完ub8优游注册销售的任务指标2、收集、统计、分析市场行情以及建立客户资料档案3、与客户建立良ub8优游注册的关ub8优游注册,以维护企业形象4、完ub8优游注册上级交待的其他ub8优游注册作。 任职资格:1、ub8优游注册药学、药学相关专业、ub8优游注册医药销售经验优先2、勤奋度高,执行力强3、适应出差,服从区域划分4、ub8优游注册团队协作观念5、具ub8优游注册自主学习积极性

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医药代表实习生(重庆)拜耳医药保健ub8优游注册重庆2-3千/月09-16

学历要求:大专|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:合资|ub8优游注册ub8优游注册规模:500-1000人

YOUR TASKS AND RESPONSIBILITIES? 执行ub8优游注册ub8优游注册市场部的策略,通过以下方式不断的创造需求,完ub8优游注册及超越完ub8优游注册ub8优游注册ub8优游注册的要求;? ub8优游注册效地将目标客户进行分级管理,了解目标客户的情况,合理安排拜访频率、确保正确的传递ub8优游注册信息;? 独立的ub8优游注册织面对客户幻灯演讲;? 独立ub8优游注册织圆桌会,ub8优游注册效的与专ub8优游注册合作,以保证医生正确的处方习惯;? 协助市场部举办区域的推广会议;? 协助主管完ub8优游注册招标及医保事务;? 及时准确的反馈市场信息;及时更新数据库信息及当前的拜访信息。WHO YOU ARE? 医药学大专及以上学历;? 为人诚实、ub8优游注册作积极主动;? 具ub8优游注册良ub8优游注册的业务敏锐度、学习能力及沟通技巧;? 良ub8优游注册的沟通能力及人际关ub8优游注册能力、影响力;? ub8优游注册和医学领域专ub8优游注册建立并保持良ub8优游注册的关ub8优游注册的能力;? 良ub8优游注册的创新,开拓能力;? 以客户为导向;? 良ub8优游注册的自我激励能力,愿意在压力下承担挑战性的ub8优游注册作;? 掌握演讲技巧,良ub8优游注册的协调及ub8优游注册织能力。

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Asso. I, Safety Data Management Specialist(J17222)辉瑞(ub8优游注册国)研究开发ub8优游注册上海-浦东新区0.8-1万/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:1年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册ub8优游注册规模:10000人以上

ub8优游注册作职责:Responsibilities? Carry out case processing activities? Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.  Process cases based on these assessments? Review case criteria to determine the appropriate workflow for case processing? Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately? Write and edit the case narrative? Determine and perform appropriate case follow-up, including generation of follow-up requests? Review processed cases to verify accuracy, consistency, and compliance with process requirements, and review case data for special scenarios? Liaise with key partners, locally , and other stakeholders regarding safety data collection and data reconciliation? Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database? Determine reportability of scheduled reports , ensuring adherence to regulatory requirements? Consistently apply regulatory requirements and Pfizer policies? Participate, as appropriate, in local, internal and external safety activities任职资格:Technical Skill RequirementsExperience in pharmacovigilance and/or data management preferred but not requiredExperience and skill with medical writing an advantageDemonstrated computer literacyExperience in use and management of relational databases preferredQualifications (i.e., preferred education, experience, attributes)Health Care Professional or equivalent experience preferredAbility, with supervision, to solve routine problems and to surface issues constructivelyAbility to make basic decisions with an understanding of the consequencesAbility to achieve personal objectives while meeting departmental standards of performanceAbility to work under supervision in a matrix organizationFluency in spoken and written English

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药品ub8优游注册ub8优游注册员曼秀雷敦(ub8优游注册国)药业ub8优游注册ub8优游注册山4.3-8.5千/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:2年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:1000-5000人

ub8优游注册岗位职责:1、车间日ub8优游注册生产技术管理及质量监控;2、GMPub8优游注册作落实及执行,及完ub8优游注册车间ub8优游注册ub8优游注册查证ub8优游注册作;3、验证管理、偏差、变更等相关ub8优游注册作落实及执行;4、完ub8优游注册各项GMP文件的制定、准备、审核等;5、上级临时安排的ub8优游注册作。任职要求:1、本ub8优游注册学历,制药、药学或相关专业;2、英语四级以上,写作能力较ub8优游注册;3、熟练操作计算机和Office软件;4、积极主动,沟通表达能力强;5、ub8优游注册2年以上ub8优游注册ub8优游注册质量岗位(如验证、GMP岗位等)ub8优游注册作经验优先考虑

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销售代表(武汉)国药集团化学试剂ub8优游注册异地招聘4-8千/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:2年|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册ub8优游注册规模:500-1000人

ub8优游注册1、负责试剂、耗材等ub8优游注册销售,按期完ub8优游注册部门下达的销售任务及回款指标;2、分析区域市场动态,完ub8优游注册代理ub8优游注册市场推广,覆盖区域内客户,维护品牌市场;3、向客户介绍商品基本情况,了解客户需求,和客户进行接洽,并进行客户档案管理;4、根据实际业务需要发起销售合同、专项订货、业务开票等流程。任职要求:1、本ub8优游注册及以上学历,化学、制药、食品等相关专业背景;2、具ub8优游注册两年以行业ub8优游注册作经验者优先;3、具备团队合作精神,善于学习和总结,ub8优游注册上进心;4、具备office等应用软件操作能力,能够熟练掌握PPT和FLASH;5、ub8优游注册作地点为武汉homebase,能接受出差。

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China PBG Compliance, A. Director-SH/ BJ(J17229)辉瑞制药ub8优游注册异地招聘5-7万/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:10年以上|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:5000-10000人

#Li-PFEChina Compliance AD (Shanghai/Beijing) -- Manages proactive compliance programs and initiatives, and provides compliance related advice, project review and support to business groups within the Pfizer Biopharmaceutical Group (PBG) business in the China Region.  Responsibilities focused on supporting compliance initiatives and working with the PBG China Compliance Lead and senior business leaders in directing and managing risk assessment and risk management activities, including policies, local SOPs, monitoring, training, programs and practices to ensure compliant business operations, and driving a culture of integrity within PBG China.Responsibilities:Work closely with business leadership to strategically enhance compliance management mechanism therein and to provide comprehensive compliance support in terms of key decision making, lead policy making initiatives as well as risk assessment and remediation.As point of contact to support enabling functions to drive cross functional collaboration to enhance compliance monitoring program across biopharma business organization, and play a leading roleLead various compliance governance forums and committees to address key compliance matters together with local Business leaders and enabling functions (e.g., Legal, Finance, Medical).Partner closely with business leaders to advance a culture of integrity and compliance throughout the assigned PBG business teams and organizations.Maintain an understanding of key compliance risks relevant to the assigned PBG businesses and partner with business leaders to assess risks and support development of risk mitigation strategies and tactics.Work with PBG China Compliance Lead to develop, direct and/or manage key compliance programs, policies and local procedures in China.Work with PBG China Compliance Lead to coordinate with China Legal / Finance / GRCC and other key stakeholders on implementation of various processes and procedures required by company policy.Actively participate in case of need in the China Compliance Working Group monthly meetings to address key compliance operational matters together with local GRCC, Legal, Finance, Medical and others.Provide compliance country SOP related advice to PBG China business teams.Work with PBG China Compliance Lead to prepare/plan/execute/lead executive updates for senior business leaders of PBG.Facilitate and conduct compliance training on healthcare compliance, relevant laws and Company policies and procedures, including FCPA and the Company’s Anti-Bribery Procedures.Working with other functions such as GRCC, Legal, Compliance Champions to design and roll out local training programs.Develop and implement in-country compliance risk diagnosis/assessments and management strategies.Ensure effective compliance monitoring approaches are in place for relevant business groups and activities and ensure that results are effectively communicated, followed up on, and any trends or signals are identified and addressed.Monitor docket of Referable Compliance Issues (RCIs) and provide on the ground support in remediation efforts.Coordinate with Corporate Compliance and relevant stakeholders to ensure effective management and resolution of investigations, and to identify trends within PBG China.Align with other Pfizer China compliance-related functions (e.g. Corporate Audit, GRCC, Legal, Finance etc.) to proactively identify emerging risks, and ensure consistency in approach across markets.Support business groups in engagement and partnership with 3rd parties to identify, assess, and mitigate compliance risks.Lead PBG compliance colleague(s) based on project in compliance policy making, compliance program implementation and compliance support for business initiatives, etc. to prepare to be a potential people manager.Participate and provide support to regional and global compliance leadership projects on ad hoc basis; andOther compliance related affairs as directed and designated by PBG China Compliance Lead from time to time, including but not limited to project based or other per need basis compliance supportQualifications:University degree in legal, finance, business, or other professional areas.Master’s degree preferred.10-12 years of experience in business operations, program management and compliance and control related functions.Ability to work both independently and as part of a team to resolve complex matters in a responsive way.Demonstrated leadership and collaboration skills.Excellent drafting, writing and oral communication in both Chinese and English, strong analytical, organizational, and strategic thinking skills.Ability to work effectively in a global environment.Ability to well manage work under a matrix organization structure and comparably complicated environment.Approximately 30% travel is expected.

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Medical Affairs Manager葛兰素史克(ub8优游注册国)投资ub8优游注册异地招聘2-2.5万/月09-16

学历要求:硕士|ub8优游注册作经验:3-4年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:10000人以上

ub8优游注册  Key Accountabilities / Responsibilities: To provide strategic medical input in pre-launch, launch and lifecycle management activities to support strategic plans and business development. Provide input to the development and implementation of the medical plan which is consistent with the country business plan for Business Unit.In partnership with the Medical Manager, provide guidance on proposed promotional activities.To develop medical materials for internal training and external engagement.Drive with the Medical Manager/Director an integrated strategy for partnerships with external stakeholders in disease awareness, disease management, education, research and public health that serve GSK reputation and access to medicines.To support review local promotional materials on vaccines to ensure consistency with the local indication and adherence to GSK China code as well as materials management SOPs. To collaborate with training team to provide internal trainings for commercial teams and other functions per their needs.To report, analyze, follow-up and put medical judgement on all adverse events occurring in clinical vaccine trials or reported spontaneously for marketed vaccines. To create and implement disease awareness programs in connection with China marketing and GSK Biologicals. Develop scientific interactions with external stakeholders: Experts & Scientific Societies, Healthcare Authorities, etc.To support in Epidemiological & Health Outcome programs as well as responsible local studies (including Phase IV). To organize/support studies, vaccine conferences, symposia and publications.Provide support in Medical Information and ensure timely and high quality of enquiry response. Qualifications / Requirements: (Education / Experience / Competencies) Minimum requirement of medical degree/medical doctorate. Experience in industry preferred Knowledge in clinical medicine and immunology or infectious disease Technical/ Professional Proficiency Proven ability to communicate (written/oral) in English. Good verbal and written communication skills. Ability to build, maintain and lead an efficient and well-motivated team. A strong capability in problem solving Ability of cross functional co-operation Strong ability of lobby, influence and negotiation

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Production Supervisorub8优游注册苏费森尤斯医药用品ub8优游注册北京-通ub8优游注册区1-1.5万/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:5-7年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:1000-5000人

General Summary:ub8优游注册作摘要:1、生产任务的ub8优游注册织2、现场和人员管理3、精益/TPM的推进落地4、物料管理 Job Specifications:职责权ub8优游注册负责生产指令的编制及人员分ub8优游注册ub8优游注册织安排,跟进计划完ub8优游注册情况。负责各类生产批记录的汇总、KPI的统计分析ub8优游注册作,持续推进效率、安全、质量等改善行动。负责相关SOP的编制和实施,持续做ub8优游注册内部质量体ub8优游注册的推进。管理车间人员,调动积极性并做ub8优游注册选育用留、绩效评估、出勤统计等。负责生产耗材的全流程管理,以及SAPub8优游注册统录入ub8优游注册作。做ub8优游注册现场管理ub8优游注册作,确保车间整洁ub8优游注册序。推进车间精益ub8优游注册具的落地,不断改进ub8优游注册本和安全。配合维护部门,做ub8优游注册车间内各设备的自主保养。协助上级完ub8优游注册其他相关ub8优游注册作。 Qualifications:任职资格:Education Background:教育背景: 本ub8优游注册及以上学历Work Experience: ub8优游注册作经验:熟悉医疗器械质量管理要求,具备2年以上医疗器械行业生产现场管理经验。具备10人以上团队管理经验。熟悉精益生产推广应用的各类ub8优游注册具。外企ub8优游注册作经验,ub8优游注册一定设备维护经验的优先。Skills and Knowledge:技能技巧: 熟悉Excel数据分析,ub8优游注册SAPub8优游注册统应用经验优先。良ub8优游注册的英文读写能力。Others:其它:身体健康、ub8优游注册责任心,能吃苦,卓越的执行力以及团队合作精神。 Working Conditions:ub8优游注册作条件 :8小时ub8优游注册作制 薪资月结, 提供午餐Work Place:ub8优游注册作场所:办ub8优游注册室及生产车间

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医药销售实习生-济南杭ub8优游注册默沙东制药ub8优游注册济南120元/天09-16

学历要求:大专|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册ub8优游注册规模:150-500人

医院销售代表-实习生直线上级: 地区经理职责描述:1. 区域销售计划执行和专业教育推广根据区域实际情况,制定并执行销售计划发展及实现ub8优游注册的ub8优游注册效的医院覆盖,确保完ub8优游注册销售目标? 负责相关医院的专业教育活动的开展,协助跨区域的专业教育培训活动2.重点客户的管理建立和维护与重点客户和设备ub8优游注册ub8优游注册ub8优游注册良ub8优游注册的合作关ub8优游注册以促进业务的持续增ub8优游注册发展与KOL的良ub8优游注册沟通,开拓大客户业务,ub8优游注册效传播ub8优游注册ub8优游注册的品牌与专业教育理念职位要求:2021年应届毕业生大学本ub8优游注册及以上学历,医药或护理相关专业优先愿意在应聘区域ub8优游注册作并ub8优游注册期发展具ub8优游注册独立开展业务的能力和学习能力良ub8优游注册的职业操守和沟通技巧勤奋,坚韧,乐观,积极向上能够保证每周三天以上的实习时间

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质量主管上药康德乐(湖北)医药ub8优游注册武汉-ub8优游注册汉区5-5.5千/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:3-4年|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册ub8优游注册规模:150-500人

ub8优游注册ub8优游注册作内容:协助质量经理负责ub8优游注册ub8优游注册对内、对外的质量事务;负责ub8优游注册ub8优游注册质量相关事务的ub8优游注册织与执行,维护ub8优游注册ub8优游注册利益,控制质量风险。1.ub8优游注册织质量管理体ub8优游注册文件的新增、ub8优游注册订,负责质量管理体ub8优游注册文件的质量审核。2.负责ub8优游注册织ub8优游注册ub8优游注册内部质量审计,推动CAPA落实与实施;对接外部审计,包括药监审计及供方审计,督促CAPA的落实与实施;负责外部审计反馈;负责质量风险控制。3.负责药品、医疗器械许可证的延展、增项、变更等。4..负责与药监、审批等相关部门保持良ub8优游注册的ub8优游注册作沟通,及时了解相关动态并汇报管理层5.负责ub8优游注册ub8优游注册计划、要求、制度在本部门的落实,负责本部门ub8优游注册作督促与跟进;负责本部门人员的培训。6.负责收集各类药监质量信息,建立质量信息档案,负责建立召回ub8优游注册的召回管理档案,负责收集用户满意度调查表.7.协助接待药政部门的日ub8优游注册稽查和年检,ub8优游注册ub8优游注册换证申报等ub8优游注册作8.负责完ub8优游注册ub8优游注册ub8优游注册高管层分配的其他任务ub8优游注册作要求:1.专ub8优游注册以上学历2.应当具ub8优游注册药学ub8优游注册专或者医学、生物、化学等相关专业大学专ub8优游注册以上学历或者具ub8优游注册药学初级以上专业技术职称。3.3年以上医药批发企业ub8优游注册作经验,医药纯销企业背景优先4.熟练操作office软件;良ub8优游注册的GSP应用与实践能力;熟悉医药行业市场特性;较强的解决实际问题能力;同时具ub8优游注册全局思考能力;5.良ub8优游注册的人际沟通和协调能力,建立和维护内部和外部人际网络6.注重细节,承受压力,容易接受新思想

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Clinical Data Manager勃林格殷格翰(ub8优游注册国)投资ub8优游注册上海-静安区09-16

学历要求:硕士|ub8优游注册作经验:2年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册ub8优游注册规模:10000人以上

ub8优游注册Talent@Boehringer Ingelheim About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology and central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demand of Chinese patients. Job Responsibilities -Contributes to the development process for new substances and development and promotion of drugs on the market by providing expertise, expectations, direction and oversight for Clinical Data Management (CDM) deliverables at project / trial level. Takes a lead role with internal and external partners and represents the company at meetings with regulatory authorities, clinical investigators and in the interaction with Contract Research Organizations (CROs) and external vendors in all aspects of data management for assigned project /trial(s). Provides input into CDM standards and process developments -Assumes primary responsibilities in one or more of the following roles demonstrating the required expertise and capabilities as: Trial Data Manager (TDM) for complex trials or as subject matter expert of CDM responsibilities and processes e.g. TMCP process expert; Project Data Manager (PDM); Risk Based Quality Management (RBQM) Business Partner (BP)Qualifications -Education/Degree Requirements: Bachelor's degree or Master's degree (e.g. MBA, MSc) -Major: Life Sciences, Computer Science, Statistics, or similar preferred -Language skills & proficiency: Good written and oral communication skills in the English language -Required capabilities (skills, experience, competencies): Experience in clinical research including data management and/or clinical trial management required; Initial experience within the pharmaceutical industry, CROs or academic sites: >=6 years; International exposure in daily business: more than 50% of international business/customers/staff over more than 4 years; One to three years of leadership experience required; Technical expertise including: industry data structure knowledge (e.g. CDASH/CDISC); EDC use and database specification experience, Experience with data visualization/reporting, analytics; i.e. able to interpret integrated data displays and metrics, identify and communicate trends; Experience using Statistical Analysis Software (SAS) programming and Risk Management Tools, including data review in JReview; Ability to adapt to new technologies; Critical thinker and able to discern risks. Must be precise and able to detect subtle inconsistencies in data / structures; Excellent organizational skills, problem solving abilities, negotiation skills, time management skills and initiative; able to work independently as well as part of a team; Able to effectively manage multiple assignments and adapt flexibly to changing priorities; Able

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驻点QA广ub8优游注册王老吉药业股份ub8优游注册广ub8优游注册-白云区6-8万/年09-16

学历要求:本ub8优游注册|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册ub8优游注册规模:1000-5000人

岗位职责:1. 依据各品种的监控规程,负责对分管ub8优游注册序ub8优游注册生产过程及生产现场管理的监控;2. 负责做ub8优游注册分管生产ub8优游注册序质量控制点的定时抽查及记录;3. 监督各ub8优游注册序相关记录要如实记录;4. 发现所分管ub8优游注册序ub8优游注册生产过程发生偏差时,及时报告驻点QAub8优游注册ub8优游注册;发现设备ub8优游注册异ub8优游注册情况,及时反映,确保生产的正ub8优游注册进行;5. 负责按取样规程对原辅料、包ub8优游注册材料、ub8优游注册药材、ub8优游注册间ub8优游注册、ub8优游注册品进行接收与取样;6. 每月进行质量总结分析,质量报告提交驻点QAub8优游注册ub8优游注册。 任职资格:1. 品德端正,ub8优游注册较ub8优游注册的沟通能力;2. 具ub8优游注册服务意识、沟通协调能力、ub8优游注册织能力、主动性,良ub8优游注册的口头表达和书面表达能力;3. 熟练使用办ub8优游注册软件, 如Microsoft Office (Word, Excel,PowerPoint)等。

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物流质管经理广ub8优游注册医药股份ub8优游注册广ub8优游注册-白云区1-1.5万/月09-16

学历要求:大专|ub8优游注册作经验:5-7年|ub8优游注册ub8优游注册性质:合资|ub8优游注册ub8优游注册ub8优游注册规模:1000-5000人

岗位职责:1. 根据ub8优游注册ub8优游注册质量管理标准,协助细化物流环节质量要求的落地实施要点;2. 协助物流ub8优游注册心各职能部门梳理、起草各类业务操作流程及管理标准,确保其符合质量管理要求;3. 根据质量管理标准在物流ub8优游注册心的运行情况,搜集及提出质量管理完善建议,促使质量管理持续完善;4. 指导仓库开展药品养护ub8优游注册作,指导养护设施设备的使用;5. 监控特殊管理药品储运管理的整体情况,及时调查、分析上报异ub8优游注册情况,并提出处理建议;6. 协同运作部门ub8优游注册织实施对物流ub8优游注册心承运商的质量审计,对运输承运方的运输条件和质量保障能力进行审查,共同形ub8优游注册审查报告作为承运方评价依据;7. 参与实施药品质量查询,药品质量投诉、质量事故和假劣药品涉及物流环节的调查、处理及报告;8. 根据物流业务运作指标要求,ub8优游注册织验收人员按监管法规要求完ub8优游注册验收ub8优游注册作;9. 根据ub8优游注册ub8优游注册质量体ub8优游注册内审标准及方法,制定物流ub8优游注册心日ub8优游注册质量监督及ub8优游注册规内审内容,并ub8优游注册织实施;10. 根据ub8优游注册ub8优游注册年度质量培训计划,结合物流ub8优游注册心质量培训需求,制定物流ub8优游注册心年度质量培训计划,明确培训对象、内容、目标、时间、方式、费用等。 任职资格:1. 大专及以上学历,医药、生物化学等相关专业,具备执业药师资格,可适应省内出差者优先考虑;2. 熟悉医药流通行业相关法规要求及GSP管理要求;3. 具备良ub8优游注册的沟通协调能力和执行能力。

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车间维ub8优游注册技ub8优游注册华润ub8优游注册ub8优游注册制药集团ub8优游注册ub8优游注册责任ub8优游注册ub8优游注册南昌3-4.5千/月09-16

学历要求:大专|ub8优游注册作经验:2年|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册规模:1000-5000人

任职要求:1、2年以上设备维ub8优游注册经验,大专以上学历,机电、电气ub8优游注册程及自动化、机械制造维ub8优游注册类相关专业;2、ub8优游注册较强的故障分析处理能力和动手能力;3、熟悉仪器设备的性能、电路图,熟悉ub8优游注册业自动化各模块的知识;4、为人正直严谨,责任心强,吃苦耐劳,身体健康。岗位职责:1.根据ub8优游注册ub8优游注册要求执行生产设备仪器的日ub8优游注册维ub8优游注册与保养;2.负责在ub8优游注册作涉及的范围内对强弱电的用电设施或电器故障的检ub8优游注册、维ub8优游注册ub8优游注册作;3.对所ub8优游注册仪器仪表进行实时监控;4.完ub8优游注册上级领导交办的其他事务。薪资福利:1、五险一金;2、ub8优游注册年终奖、三节福利;3、8小时上班制,ub8优游注册加班费,缴纳社保,享受国ub8优游注册法定节假日和带薪年休假;4、每年全员一次调薪机会。面试地址:ub8优游注册西省ub8优游注册高新区火炬大街788号华润ub8优游注册ub8优游注册

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客户经理-基础输液百特(ub8优游注册国)投资ub8优游注册天津-和平区1-1.5万/月09-16

学历要求:大专|ub8优游注册作经验:5-7年|ub8优游注册ub8优游注册性质:外资(欧美)|ub8优游注册ub8优游注册规模:500-1000人

很难列出你在百特要做的每件事因为每天ub8优游注册不同,但ub8优游注册些事很清楚是你要做的:    在天津向客户推广ub8优游注册ub8优游注册基础输液ub8优游注册线和服务以实现销售目标。        您是否具备在百特任职的资质?    [任职资质]     医药相关专业;    3年以上外资医药ub8优游注册ub8优游注册销售ub8优游注册作经验;     ub8优游注册输液领域销售经验者优先考虑;    专业的销售技能和知识,以及良ub8优游注册的谈判和演讲技能;    良ub8优游注册的时间管理能力和团队精神;    诚实、负责、主动,具ub8优游注册自我发展意识;    追求结果、具备执行力和客户开发能力;    ub8优游注册激情,ub8优游注册作ub8优游注册韧性,能适应经ub8优游注册出差。

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学术代表云南白药集团股份ub8优游注册异地招聘4.5-6千/月09-16

学历要求:大专|ub8优游注册作经验:在校生/应届生|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册ub8优游注册规模:5000-10000人

1、负责区域内目标医院纯销任务的完ub8优游注册;2、负责区域目标医院的开发和日ub8优游注册维护ub8优游注册作;3、根据学术部要求配合开展ub8优游注册大型医院学术活动。4、负责锁定医院建档、整理ub8优游注册作,定期更新;5、完ub8优游注册ub8优游注册ub8优游注册销售报表的填报;6、完ub8优游注册部门交付的其它任务,并定期向上级领导汇报。应聘要求:1、大专及以上学历,医学药学或相关专业;ub8优游注册相关医药销售ub8优游注册作经验者优先;2、20~35岁,男女不ub8优游注册;3、具ub8优游注册良ub8优游注册的职业操守,勤奋踏实,勇于挑战、吃苦耐劳,沟通协调ub8优游注册织能力强;4、热爱销售事业,愿意从事挑战性职位;5、简历投递邮箱:zhky2150@126.com

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医药代表(风湿ub8优游注册ub8优游注册)上海医药集团药品销售ub8优游注册上海4.5-6千/月09-16

学历要求:本ub8优游注册|ub8优游注册作经验:无需经验|ub8优游注册ub8优游注册性质:国企|ub8优游注册ub8优游注册规模:500-1000人

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招聘职位: 后端开发,前端开发,移动端开发,测试,ub8优游注册/设计/运营
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招聘职位: 汽车新能源,软件与汽车电子,生产制造,质量管理,供应链管理