北京PK10人工在线计划

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Senior Channel Strategy Manager勃林格殷格翰(中国)投资有限公司上海-静安区09-08

学历要求:大专|工作经验:5-7年|公司性质:外资(欧美)|北京PK10人工在线计划公司规模:10000人以上

Talent@Boehringer Ingelheim 关于人用药品业务勃林格殷格翰的医药研发能力在业界全球领先。我们不断探索全新的医学突破,提供创新药物来满足患者在心血管疾病、呼吸疾病、代谢疾病、免疫学、肿瘤学和中枢神经系统疾病这些关键治疗领域的需求 。不久的未来,公司将上市十余种创新产品以满足中国患者的需求。 工作职责 The position is responsible for developing national commercial channel strategy, build up strategic partnership with distributors through monitoring, evaluating and coaching them for further improvement with compliance 该位置负责制定全国商业渠道策略,通过对经销商进行监控和评估以及培训与其建立互信互利的合作伙伴关系,以确保经销商以及商业渠道在合规的前提下发展 1.Develop strategic plan for broad market, drug store market, distribution channel and business development with a solid link to corporate strategy and track its implement 根据医药市场,药店以及经销商渠道的业务协作制及发展定全国渠道战略计划并跟进执行 2. Integrate distribution channel to implement effective management and evaluation, to identify strategic developing plan 整合经销商渠道并对其进行有效管理,评估并制定战略性的发展计划 3. Ensure BI business development through monitoring all distributors inventory, return goods and commercial rebate 通过对经销商库存,退换货以及商业补偿实施监控确保BI业务的稳定增长 4. Lead team for sales data analysis, invoice sales and DSO to optimize allocation of resources 带领团队分析销售数据,invoice sales和DSO以优化资源配置 5. Organize distribution conference and commercial policy training to develop distribution channel conforming to BI SOP 筹划经销商会议并培训商业政策使渠道经销商发展的同时符合公司的各项流程制度 任职条件-学历: 大专学历以上-专业: 医学或药学背景为佳-所需的技能:良好的跨部门协作和沟通,团队协作精神,-语言能力:英语流利-所需的工作经验背景:5年及以上医药行业销售, 政府事务及渠道工作经验,需要有团队管理经验,熟悉销售运营,擅长数据分析,同时需要有策略制定的能力

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Sr Medical Compliance Manager/资深医学合规经理罗氏诊断产品(上海)有限公司北京09-08

学历要求:本科|工作经验:8-9年|公司性质:外资(欧美)|公司规模:1000-5000人

You will be responsible to review promotional material and study from medical regulatory prospective; provide direction and optimization of local process to clinical operation function, following NMPA regulations, RDSL SOPs and Divisional Standards. Conducting clinical quality control activities, according to the relevant NMPA and global regulations, guidance, standards and RDSL SOPs; conducting training needs analysis, training plan development, supervising the implementation of training of local clinical operation function. Handling medical regulatory inquiry from other departments and coordinate cross-functional project. 根据NMPA法规,RDSL SOP 和DS的要求,从医学法规角度审阅推广材料和临床研究;向临床运营职能提供本地流程的指引和优化。根据NMPA和全球法规、指南、标准及RDSL SOP开展临床试验质量控制活动;针对临床运营团队进行培训需求分析,培训计划制定及监督培训的执行。处理来自其他部门的医学法规问询,参与跨部门项目。 Main Tasks & Responsibilities主要工作职责: 1. Reviewing corresponding event applications to make sure compliance with Dia Symphony and related SOP's, Good Clinical Practice (GCP) and HCP guidelines; Reviewing HCP PPTs and Roche promotion materials to ensure no off-label promotion. 审核相应的活动申请,确保符合Dia Symphony及相关SOPs,临床试验质量管理规范(GCP)和HCP指南;审核HCP幻灯和罗氏诊断产品推广材料以确保无适应症外推广。 2. Conducting clinical quality control activities, according to the relevant NMPA and global regulations, guidance, standards and RDSL SOPs. 根据相关的NMPA及全球法规,指南,标准和RDSL SOP,开展临床试验质量控制活动。 3. Assisting clinical operation function, providing direction and optimization of local process according to the requests of Divisional Standard, GCP and QC observation. 根据DS,GCP和QC观察发现,协助临床运营团队提供对于本地流程的优化和指导。 4. Leading training needs analysis, planning development, supervising the implementation of training of local clinical operation function. Providing training of clinical trial quality related topics as needed. 主导临床运营团队进行培训需求分析,培训计划制定,监督培训的执行。如需要,提供临床试验质量相关的培训。 5. Developing and adopting the IT systems and tools to facilitate and standardize the local clinical operation process, together with the supports of local IT and global counterparts. 在本地IT及全球同行的支持下,开发并采用IT系统和工具以促进本地临床运营过程的标准化。 6. Developing and maintaining a good working relationship with BAs and other dept. to support the cross-functional projects. 与BAs和其他部门发展并维护良好的工作关系,支持跨部门项目。 7. Developing career and development plan for subordinates. 为下属规划职业发展计划。 Basic Requirements of the Job基本任职资格: You should hold at least Bachelor degree in medical science degree, preferably in clinical medicine, medical laboratory, pharmacy administration, pharmacology, and biology. 医学相关专业本科及以上学历,临床医学、医学检验、药事管理、药学、生物学优先 You should have: 1. Proficiency in both spoken and written English. Good command of MS office software application; 熟练掌握英语口语及书面表达,熟练应用微软办公软件 2. Understand pharmaceutical and/or medical device regulation; 了解药品及/或医疗器械法规 3. At least 8 years of working experience in clinical medicine, pharmaceutical, Medical Device, or in-vitro Diagnostics industry, and 3 years of working experience in medical compliance, clinical trial quality management. At least 5 years of project management or people leader experience are preferred. 8年以上临床医学、制药、医疗器械或体外诊断行业工作经验, 3 年以上医学合规、临床试验质量管理相关经验,至少5年以上项目管理或人员团队管理经验者优先。

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Sr Clinical Trial Materials Mgmt Manager礼来(上海)管理有限公司上海09-08

学历要求:|工作经验:无需经验|公司性质:外资(欧美)|公司规模:1000-5000人

北京PK10人工在线计划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 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.RESPONSIBILITIES:The Mgr/ Sr. Mgr, Clinical Trial Material Management is responsible for clinical trial (CT) material coordination (inclusive of investigational product, commercial materials, and ancillary supplies) in partnership with the global Product Delivery organization and clinical development to support regional clinical trials in accordance with Lilly procedures, local laws and regulations.The Mgr/ Sr. Mgr, Clinical Trial Material Management partners internally and externally to develop strategies that enable the on-time delivery and stable supply of CT materials to support clinical development in their region.Primary Responsibilities:This job description is intended to provide a general overview of the job requirements at the time it was prepared.The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description.Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.1. LeadershipResponsible for clinical trial material coordination and support for regional clinical trial development which can include local clinical trials, regional participation in global trials, investigator initiated reseach, and expanded access programs.Acts in conjunction with clinical development teams and Product Delivery personnel to develop robust strategies for and implement clinical trial material management activities for their region.Be a key contributor to compound-level and trial-level strategic decisions as it relates to CT materials and as applicable to their region.Identify and communicate with Product Delivery, Clinical Development, and the affiliate potential risks, limitations, and mitigation/contingency strategies (where appropriate) associated with the CT material supply for supported compounds/studies.Work with Product Delivery to ensure robust supply chain strategies are developed for all in-scope studies in region.Build relationships with internal and exernal partners and ensure robust communication with those partners them as it relates to CT materials.2. Technical ExpertiseTechnical expert in local sourcing, laws and regulatorions, and import/export rules for ancillaries and commercial prodcutsUnderstand commercial product sourcing strategies and processes for managing.Support ancilliary supplies in accordance with local regulations.Apply knowledge of supply planning methodologies and expertise in supply chain principles to regional supply chain strategy and process improvement.Support selecting and qualifying contract manufacturing organizations (CMOs) with the needed capabilities, when required.Provide technical oversight and in-country support for overseeing the contract manufacturing, packaging, labeling, and distribution activities, when needed, including including batch record development and execution and shipping documentation preparation. Serve as person in plant to provide oversight and guidance, as needed.3.DeliveryResponsible for the on-time delivery and management of the CT material supply and related information from the initiation of study planning through approval of the final study report for their associated studies.Partner with a network of internal resources and third party contract organizations to execute development activities as it relates to CT suppliesProvide documentation to support importation, exporation, quality release, and distribution activites.Ensure compliance with appropriate Lilly procedures, local regulatory requirements, and local laws in their region as it relastes to clinical trial materials.Aid in issue resolution as it relates to CT material deliveryAct as a point of contact for recalls and destruction of clinical trial materials which do not meet quality standards within region, as needed.Accountable for appropriate escalation of issues and potential countermeasures to Product Delivery and the clinical teams.Leads the interpretation of relevant regulations and guidelines and acts as a contact person in the affiliate(s).4. Continuous ImprovementUnderstand performance metrics related to CT material for region and identify areas for improvement and simplification.Ensure SOPs for CT materials are well understood across the affiliate(s), leading and providing clarification on local implementation.Support the development of global SOPs for CT materials to maintain alignment with local laws and regulationsd. Influence the quality system at affiliate level to meet regulatory expectation and business needs.Responsible for solving broad based and project-specific technical and business issues.f. Continuously assess business processes for inefficiencies and improvement opportunities, identify action plans, and implement improvements.Document the regional processes as it relates to CT materials including the creation and update of procedures, tools, reference documents and process maps, as appropriate.Document deviations to procedures, conduct root cause analyses, and leverage learnings to drive improvements and simplificationCommunicate process improvements, industry trends, new technologies, and new capabilities to stakeholders.Minimum Qualification Requirements:-Bachelor’s degree preferably in a scientific or health-related field.-More than 5-8 years of pharmaceutical development experience.-Experience managing inventory/supplies or complex supply chains.-In-depth knowledge of clinical research, clinical trial manufacturing, packaging and/or distribution, and interactive response systems (IRS).-Ability to use and apply multiple computer applications, especially Excel and Microsoft Project.-Demonstrated project management skills.-Experience working and communicating with third party contract organizations.-Fluent spoken and written English skills.-Other Information/Additional Preferences:-Experience (5+ years) managing clinical trial materials, complex supply chains, and/or cross-functional projects.-Advanced degree (Master, Doctorate, etc.) in operations management, supply chain, or a scientific field-Degree, certification, or equivalent experience in project or supply chain management (i.e. APICS).-Demonstrated ability to build and foster teamwork.-Excellent interpersonal and organizational skills.-Ability to influence at many levels and across disciplines, both internally and externally.-Ability to manage multiple tasks and respond to changing priorities.-High initiative, learning agility and a flexible, positive attitude.-Strong quantitative skills and expertise.-High degree of accuracy and attentive to details.Ability to proactively identify problems and work toward a solution.Demonstrated leadership and broad expertise within the clinical trial material services organization.Ability for international travel to support development and integration with global partners (up to 10%).Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.职位要求:详情请见职位描述

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化学分析工程师纽迪希亚制药(无锡)有限公司无锡-无锡新区09-08

学历要求:本科|工作经验:2年|公司性质:外资(欧美)|公司规模:500-1000人

北京PK10人工在线计划Be responsible for chemical analysis work in chemical lab.  负责化学实验室的化学分析工作。 Take the responsibility for the chemical analysis to ensure that test report are available within target day.  负责原料和成品的化学分析,确保在规定的时间完成检测。  Support vary validation including analysis method, product validation and equipment validation to provide valuable data and report.  支持验证工作以提供有效的数据和分析报告,包括方法学验证、产品验证、设备验证等。   Ensure that equipment and glassware are well managed and maintained to meet test requirement.  负责仪器及玻璃量器的管理维护,确保满足实验要求。  Take the responsibility for reporting deviation and assist OOS investigation.  负责检验异常情况汇报,并协助OOS的原因调查分析。 Deploy on job training for new employee. 开展新员工岗位操作培训。  Education & working experience 学历与工作经验要求:  Bachelor degree or above(scientific/technical), Analysis or related background  大学本科工程类(或科学技术)以上学历,分析专业或相关背景。  Good drug analysis knowledge  良好的药品分析知识  Occupational qualifications职业资格要求:  Proficient English communication skill (written and verbal)  良好的英语听、说、读、写能力。  Excellent MS office skills  能够熟练使用办公软件够熟练使用办公软件。  Others其他:  Easy communication, good team player.  良好的沟通能力和团队合作精神。

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医学影像员(权属三级公司)拉萨市城市建设投资经营有限公司拉萨6-9千/月09-08

学历要求:本科|工作经验:2年|公司性质:国企|公司规模:5000-10000人

1.医学影像学专业,本科及以上学历;2.具备DR、CT等诊断能力,可独立操作影像诊断仪器,有2年以上工作经验者优先。

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质量管理员上海嘉和诚康医疗器械有限公司上海-浦东新区5-5.5千/月09-08

学历要求:大专|工作经验:2年|公司性质:上市公司|公司规模:50-150人

北京PK10人工在线计划工作内容:1. 负责首营企业、首营品种和客户资质资料的初步审核和归档并进行动态管理;2. 负责质量信息收集传递;3. 负责医疗器械质量信息档案的建立;4. 协助上级领导完善质量管理体系,监督、执行、核查质量体系运行情况;5. 负责计算机系统基础数据的维护;6. 完成领导布置的其他工作任务。7. 医学检验相关专业,有医疗器械质量管理、生产或研发工作经验者优先。

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仓管员海雅美生物技术(珠海)有限公司珠海-金湾区3-4.5千/月09-08

学历要求:中专|工作经验:1年|公司性质:外资(非欧美)|公司规模:150-500人

要求***性,20岁以上,专业不限,中专以上学历,会办公软件及ERP操作系统,有一年以上仓库管理工作经验,医业行业相关工作经验者优先;能接受适度轮岗、调岗。工作内容:1、物料收发存管理2、产品收发存管理3、ERP系统账务管理4、仓库现场5S整理;

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学术项目支持江苏和泽干细胞基因工程有限公司南京-江宁区0.9-1万/月09-08

学历要求:硕士|工作经验:无需经验|公司性质:上市公司|北京PK10人工在线计划公司规模:500-1000人

北京PK10人工在线计划1.生物或分子学相关专业,硕士(含)以上学历;2.负责公司日常的学术支持、项目申报等工作;3.负责江苏省内学术交流、产品知识推广等;4.负责公司新员工入职培训;5.有较强的学习能力、良好的沟通能力、表达能力及团队合作精神;

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细胞、病毒培养技术主管苏州西山生物技术有限公司苏州-工业园区0.8-1万/月09-08

学历要求:本科|工作经验:1年|公司性质:合资|公司规模:少于50人

1.组织开展负责实验室常用抗原制备、质量控制及结果分析工作;2.组织sop等文件编写和修订,监督日常检测质控和组织质量比对;3.负责实验室的组织管理工作,人员培训及绩效考核;4.负责跟踪新技术和开发新项目;5.完成领导交代的其他工作事项。岗位要求:1.生物学相关本科或以上学历; 2.有细胞、病毒培养、蛋白纯化一年以上经验者优先;3.熟悉免疫学实验及抗原质量控制工作;4.良好的英语阅读/表达和沟通能力;5.富有进取心和责任心,优秀的组织能力,部门管理能力和沟通能力;6.具有主动学习能力和创新精神,提升工作效率或优化流程。

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采购专员江苏海泽医疗科技发展有限公司无锡-锡山区4.5-6千/月09-08

学历要求:大专|工作经验:3-4年|公司性质:民营公司|公司规模:50-150人

1、采购生产用的原材料、辅料,采购订单管理及在库数量控制;2、能根据生产计划的变化,及时与供应商联络,调整仓库出入库时间;3、供应商回来产品出现品质问题,及时联络供应商处理;4、协助财务与供应商对账、整理发票、请款;5、整理当月的才后数据,将当月生产用的主原料信息汇总,向领导汇报;

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药店营业员(至善路药房)南京上元堂医药股份有限公司南京2-6千/月09-08

学历要求:大专|工作经验:1年|公司性质:上市公司|北京PK10人工在线计划公司规模:150-500人

北京PK10人工在线计划岗位职责:1、接待顾客的咨询,了解顾客的需求并达成销售;2、负责做好货品销售记录、盘点、账目核对等工作,按规定完成各项销售统计工作;3、完成药品的来货验收、上架陈列摆放、补货、退货、防损等日常营业工作;4、做好所负责区域的卫生清洁工作;5、完成上级领导交办的其他任务。任职资格:1、大专及以上学历,医药相关专业;2、有相关工作经验者优先;3、具有较强的沟通能力及服务意识,吃苦耐劳;4、年龄18-35岁,身体健康。

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小时工(信息录单员)武汉天一辉远生物科技有限公司武汉-洪山区20元/小时09-08

学历要求:|工作经验:|公司性质:民营公司|北京PK10人工在线计划公司规模:50-150人

小时工(信息录单员)          20元/小时职位信息1、工作时间:每天晚上8点至10点(20:00点至22:00),在公司办公(公司有技术人员),按小时结算,每小时20元。                    周日晚上可以休息。2、工作内容:准确无误的将纸质订单信息,录入到电脑系统。3、工资按月结算。4、个人熟练操作电脑,熟悉办公软件,细心、责任心强。5、公司地址,武大科技园(三环线边上,万科城市花园附近),有意者可电话联   系027-81621001。武大科技园航域二期B3栋17层。

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装配技工深圳市汇松科技发展有限公司深圳-罗湖区3-5千/月09-08

学历要求:高中|工作经验:2年|公司性质:民营公司|北京PK10人工在线计划公司规模:50-150人

任职要求:1、有较强工作责任感和事业心;2、手脚灵活,思维敏捷,能服从安排;3、能看懂结构图及熟练使用烙铁,万用表等相关工具;4、有医疗器械的整机装配经验者优先。居住莲塘及附近优先考虑。

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业务员(必须自备汽车)沈阳千禧浪人义齿有限公司沈阳-于洪区4-8千/月09-08

学历要求:中专|工作经验:3-4年|公司性质:民营公司|公司规模:少于50人

北京PK10人工在线计划工作职责1,沈阳市内按照区域划分,口腔门诊开发、维护。2.爱岗敬业、吃苦耐劳、有上进心、主观学习能力强。3.入场前岗位培训,专业知识培训,下市场演练。4.有责任心、长期发展者优先。5.每周一天轮休,每天早晚需要到公司签到打卡。岗位要求:男女不限,学历不限,可非口腔专业;自备汽车。具有销售经验。岗位待遇:任务底薪4000+有意者可电话咨询李经理    电话 :15712408971

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精密模切工程师上海诺瓦立医疗器械有限公司泰州6.5-8千/月09-08

学历要求:中专|工作经验:3-4年|公司性质:合资|公司规模:50-150人

北京PK10人工在线计划1、产品CAD图纸制作;  2、产品工艺、材料、评估和设计; 3、制作生产模具图;  4、对生产模具和生产工艺进行验证、检验;  5、对产品小批量试产及工艺优化改造以及生产现场做工艺技术指导,解决产线突发异常问题任职要求: 1、学历专业:大专以上,理工科,机械或机电专业优先。 2、工作经验:三年以上工作经验,有医疗器械或电子行业精密模切生产经验者优先。 3、技能要求: 1、有平刀或圆刀模切行业工程3年以上工艺革新及管理的工作经验,尤其熟悉多工位圆刀模切机贴合、异步等工艺或有医用材料精密模切工程经验者优先; 2、精通产品制作流程,能根据现有设备进行工艺和设备改善,以达成降低材料成本和提升生产效率的能力;  3、有很强的模切材料应用理论,精通材料匹配; 4、有很强的逻辑能力,善于思考,对客户或现场提出的异常,能及时分析异常并能及时改善,不断优化现有产品工艺;  5、学习能力强,工作主动,善于思考,具强烈责任心,有担当和主动改善的欲望,能承受较大的工作压力。 

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药剂师(医院)重庆亚通实业(集团)有限公司重庆-渝北区3-5.5千/月09-08

学历要求:大专|工作经验:2年|公司性质:民营公司|北京PK10人工在线计划公司规模:500-1000人

要求:1、大专学历以上,药学相关专业,中医、西医各两名;2、能吃苦耐劳,爱岗敬业,团结他人,遵守规章制度;3、有一定的工作经验,持证者优先。***联系电话: 86871299  曹老师

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文控专员深圳青澜生物技术有限公司深圳-龙华区6-8千/月09-08

学历要求:中专|工作经验:3-4年|公司性质:民营公司|公司规模:50-150人

北京PK10人工在线计划1、负责公司体系文件资料的管理,对各部门文件资料工作进行监督、检查;2、负责受控文件的会签、评审、编号、分发的监督和实施;3、负责文件的保存、整理、保存期限的监控;4、负责制度文件和技术文件、整理、分类、鉴定、保管、保护、分发回收等工作;5、严格执行保密制度,做好文件资料密级划控和守密工作。

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营业员上海万芸药房连锁有限公司上海-嘉定区3-6千/月09-08

学历要求:|工作经验:|公司性质:民营公司|公司规模:50-150人

1、药品柜台销售,提供药品咨询、销售服务。 2、负责做好所在门店盘点等工作,按规定完成各项销售任务 3、完成商品的来货验收、上架陈列摆放、补货、退货、防损等日常营业工作; 4、做好所负责区域的卫生清洁工作; 5、完成店长/店助交办的其他任务。6、底薪+高提成。任职资格: 1、中专以上学历;医学、药学、护理等医药相关专业优先。 2、有连锁药房相关工作经验者优先; 3、具有较强的沟通能力及服务意识,吃苦耐劳; 4、无工作经验,公司负责培训!

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合成研究员西安万隆制药股份有限公司西安6-8千/月09-08

学历要求:本科|工作经验:1年|公司性质:民营公司|北京PK10人工在线计划公司规模:150-500人

有机化学,药品合成1、本科及以上,有机化学相关专业,熟悉有机合成基本操作;2. 良好的中英文科技论文阅读和写作能力3. 具有一年以上有机合成研究背景4. 工作勤奋、踏实,有团队协作精神。

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销售经理(口腔医疗)郑州德派医疗器械有限公司郑州-高新区2.5-3万/月09-08

学历要求:大专|工作经验:1年|公司性质:民营公司|公司规模:50-150人

负责公司旗下高端义齿定制、口腔耗材、树脂牙、隐形正畸(美立刻)及义齿设备等产品的市场推广与销售工作;口腔医疗行业的实力企业,品牌知名度及产品品质在市场认可度较高;有二手房中介、器械和药品销售,保健品销售,保险销售,房地产销售,快消品销售,健康销售行业经验优先考虑。任职要求:(年龄30岁以下)1、有意长期从事医疗器械行业(口腔科材料),并期望自己有良好的发展;2、有良好的语言表达、沟通能力及应变能力,负责公司产品销售和推广;3、具有专业的市场分析及判断能力,有良好的客户服务意识;4、吃苦耐劳、百折不挠,具有良好的抗打击能力;5、医疗、口腔、市场营销专业优先考虑,有同岗位工作经验者俱佳;6、公司产品线全,义齿、口腔耗材、隐形正畸、义齿设备、树脂牙等;7、报销差旅费,提成另计,沉淀下来即可实现高薪;8、工作区域根据公司具体安排,有意向需面谈。面试地址:西三环大学科技园东区7号楼8层,(广告勿扰,暂不需招聘渠道)新公司即将搬迁至西四环莲花街,亿达科技新城。销售不坐班!

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-中高端人才求职平台

招聘职位: 后端开发,前端开发,移动端开发,测试,产品/设计/运营
招聘职位: 财务审计,合规与风险控制,后台运营,投行,销售
招聘职位: 房地产开发,建筑工程,规划设计,商业,市场营销
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