工作職責(zé):
Why Patients Need You？
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.？？？
？
What You Will Achieve？
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for activities involved in developing and maintaining quality programs, processes？and procedures that ensure compliance with established standards and agency guidelines. In consultation with Clinical R
車艷鑫
崗位職責(zé)： 1.負(fù)責(zé)營(yíng)銷項(xiàng)目和在建項(xiàng)目的項(xiàng)目設(shè)計(jì)及技術(shù)管理管理。 配合部門負(fù)責(zé)人對(duì)公司各項(xiàng)目進(jìn)行設(shè)計(jì)及技術(shù)管理工作，主要包括項(xiàng)目營(yíng)銷和實(shí)施階段的設(shè)計(jì)管理、技術(shù)方案、施工組織設(shè)計(jì)、設(shè)計(jì)優(yōu)化，并組織解決重點(diǎn)難點(diǎn)項(xiàng)目的設(shè)計(jì)和技術(shù)問(wèn)題。 2.負(fù)責(zé)組織營(yíng)銷項(xiàng)目勘察測(cè)量專案、設(shè)計(jì)方案評(píng)審、設(shè)計(jì)優(yōu)化、施工組織設(shè)計(jì)、P6計(jì)劃的編制、審核和評(píng)審，組織實(shí)施項(xiàng)目技術(shù)策劃評(píng)審、專項(xiàng)方案評(píng)審及協(xié)助解決重難點(diǎn)技術(shù)問(wèn)題，協(xié)助區(qū)域科技研發(fā)項(xiàng)目管理。 3.與顧問(wèn)公司保持密切聯(lián)系，與第三方資源協(xié)作，有效解決實(shí)際問(wèn)題。 4.完成領(lǐng)導(dǎo)交辦的其他任務(wù)并接受短期出差。 任職資格： 1、工作年限：10年左右的工作經(jīng)驗(yàn)，5年以上海外工作經(jīng)驗(yàn)。 2、行業(yè)、項(xiàng)目經(jīng)驗(yàn)：有港口、路橋、建筑、市政行業(yè)項(xiàng)目技術(shù)管理工作經(jīng)驗(yàn)，有中東地區(qū)項(xiàng)目工作經(jīng)驗(yàn)的優(yōu)先。 3、能力、性格特質(zhì)：組織協(xié)調(diào)溝通能力強(qiáng)、有團(tuán)隊(duì)合作精神 4、教育背景：大學(xué)本科以上土木專業(yè)，碩士?jī)?yōu)先。 5、語(yǔ)言能力：英語(yǔ)流利 6、性別與年齡：45歲以下 7、其他：適應(yīng)海外工作和生活
林懿翀
崗位職責(zé):
1、負(fù)責(zé)密山市人民醫(yī)院的科室開(kāi)拓、客戶管理，完成銷售任務(wù)指標(biāo)；
2、負(fù)責(zé)產(chǎn)品在目標(biāo)區(qū)域內(nèi)的品牌策略和推廣計(jì)劃，向客戶有效傳遞產(chǎn)品信息；
3、組織學(xué)術(shù)活動(dòng)，有效的傳遞產(chǎn)品核心信息，提高產(chǎn)品在區(qū)域內(nèi)的影響力；
4、保持高水準(zhǔn)的專業(yè)化拜訪，了解客戶的醫(yī)學(xué)需求，收集反饋臨床使用情況及異議，提供有效解決方案；
5、配合處理產(chǎn)品售后服務(wù)的相關(guān)事項(xiàng)，包含但不僅限于產(chǎn)品不良反應(yīng)的反饋，提高客戶滿意度；
6、領(lǐng)導(dǎo)布置的臨時(shí)性工作。
任職要求:
1、本科以上學(xué)歷，醫(yī)藥相關(guān)專業(yè)、市場(chǎng)營(yíng)銷等專業(yè)；
2、1年及以上頭部企業(yè)及醫(yī)院相關(guān)工作經(jīng)驗(yàn)，熟悉醫(yī)藥市場(chǎng)運(yùn)作，35周歲以下。
HR
工作職責(zé):
Why Patients Need YouWe're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines.
What You Will AchieveYou will help us in preparation, publication, tracking and quality control of our submissions to the regulators in compliance with document management standards. You will be responsible for activities related to enterprise-wide regulatory management systems, including systems coordination, training others, developing and implementing plans, and providing input to systems designs.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical submissions on time. Your innovative use of communication tools and techniques will facilitate in addressing difficult issues and establishing consensus between teams.
It is your focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve ItContribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Execute, through use of standards and tools, designated operational tasks or through the applicable Pfizer country office, conforming to regulatory submission milestones and applicable regulatory obligations.
Support the interpretation of regulatory guidelines to produce business requirements and ensure that those requirements are implemented where appropriate at local/regional level.
Work with the team managers to effectively forecast and manage project specific resources utilizing flexible resourcing and global load sharing as normal business practice.
Operate as Subject Matter Expert in dossier types and processes with responsibility for training and mentoring fellow colleagues.
Escalate, inform, and resolve any issues that may impact submission builds or the logistics of global submission delivery to regional partners or Health Authorities.
Lead the implementation and execution of withdrawal strategy in partnership with regulatory strategy.
Responsible for updating the Regulatory parameters for monthly reports to local and global customers.
Supports allocated region/countries, with additional responsibility to support other locations through utilization of global tools.
Able to follow scientific arguments and ensure data is complete and sound.
Ensure maintenance of product and license information in the tracking database.
Responsible for curriculum and training assignments and assist in the collection of training metrics and produces compliance figures for distribution.
任職資格:
Qualifications
Must-Have
Bachelor's Degree
3 years of experience
Relevant experience in electronic submissions build within the Pharmaceutical Industry
Strong knowledge of the drug development process, clinical trial operations, regulatory affairs, and submission management
Understanding of systems and electronic technologies used to support submission and planning activities
Attention to detail and exceptional organizational skills
Presents scientific data effectively, in verbal and written in a logical and persuasive manner
Proven experience managing or delivering through others in a global team environment
Proficient in English, verbal and written
Nice-to-HaveMaster's degree
Relevant pharmaceutical experience of Clinical Trial or regulatory management
Familiarity with pharmaceutical organizational structures, systems, and culture
Experience in project management
車艷鑫
負(fù)責(zé)復(fù)星醫(yī)藥公司員工餐廳中西點(diǎn)心制作。
崗位職責(zé)：
1、負(fù)責(zé)員工食堂各類點(diǎn)心的制作；
2、品種質(zhì)量要求色香味俱全、成品符合食品衛(wèi)生要求；
3、根據(jù)食堂的需求提供各類早點(diǎn)：中式點(diǎn)心：包子、饅頭、花卷、生煎、水餃等；西式點(diǎn)心：面包、蛋糕,清酥,混酥,泡芙等；
4、能獨(dú)立完成中西式點(diǎn)心的制作。
5、完成上級(jí)領(lǐng)導(dǎo)交辦的其他工作。
任職要求：
1、年齡25-55歲，身體健康。
2、有相關(guān)級(jí)證書。
3、有五年以上相關(guān)工作經(jīng)驗(yàn)。
薪資福利：
1、繳納上海五險(xiǎn)一金，加班有額外加班費(fèi)
2、做五休二，6:30-15:00
3、提供工作餐和住宿
工作地點(diǎn)：
盛榮路367號(hào)，軍民路和盛榮路路口
王先生
工作職責(zé): JOB SUMMARY Summarize the primary purpose
車艷鑫
工作職責(zé): ROLE SUMMARY The Central Monitor II is responsible for ensuring the
completeness, quality and integrity of the subject data in the clinical trial
database under Risk Based Monitoring (RBM) mode. The areas of activity include
but are not limited to: developing Risk-Based Monitoring system for applicable
studies, ensuring key risk indicators (KRIs) properly defined and set up in the
system to support the study, processing and reviewing study data in the system
for the signal and action management, follow up for the issue resolution. The
Central Monitor I ensures risk based monitoring activities comply with
regulations, applicable Standard Operating Procedures (SOPs) and Processes at
all times and is familiar with supported systems (RBM system, etc.) and able to
troubleshoot and provide rapid response for all database issues. The Central
Monitor I works with the global study team to meet the study objectives. ROLE
RESPONSIBILITIES General: Implement global strategies, initiatives, processes,
and standards to ensure consistent, efficient, and quality processes to meet
quality, timelines and deliverables. Provide technical expertise to set up and
test study level Risk-based Monitoring system Review study level system outputs
to process for the signal and action management Execute communication plans
車艷鑫
任職要求：
1、基礎(chǔ)辦公軟件使用。
2、相關(guān)工作經(jīng)驗(yàn)優(yōu)先錄取。
3、細(xì)心、理解能力、學(xué)習(xí)能力強(qiáng)。
4、愛(ài)崗敬業(yè)、工作積極，能夠接受偶爾排班。
工作職責(zé)：
聽(tīng)錄音、發(fā)現(xiàn)共性問(wèn)題及時(shí)反饋。
工作時(shí)間：早9晚6，雙休
薪資待遇：3000-4000
工作地點(diǎn)：漢王制造園區(qū)二樓
華通順泰
Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveIt is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility of our clinical data. You will play an important role in processing, reviewing, and receiving patient data and records. You will be organizing clinical data forms from therapeutic groups and outside investigators. You will ensure that accurate, timely, and consistent clinical data reaches the medical department and other groups. You will be relied on for data management plans including data preparation, data validation activities, etc.As a Manager, you provide guidance to operational teams for managing projects. Your planning skills will help in preparing forecasts for resource requirements, and providing areas of improvement for products, processes or services. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams.It is your dedication and focus that will help make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItProvide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the division.Ensure work carried out by providers is in accordance with applicable Standard Operating Procedures (SOPs) and working practices.Promote the use of consistent, efficient, and quality processes to meet timelines and deliverables.Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all Data Monitoring and Management (DMM) activities and interact with Clinical Data Scientist at study level for deliverables.Serve as a technical resource to the study teams for data visualization and reporting tools and provide technical expertise and business process support in technology systems.Ensure operational excellence in collaboration with partners for application of standards, data acquisition, proactive data review and data integrity and overall data management activities.Partner with Research/Business Units and any external DM service provider to deliver high quality data management for all studies as assigned.Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions.Plan and execute communication plans and methods for engaging customer populations.QualificationsMust-HaveBachelor s Degree5 years’ experienceExperience within the pharmaceutical industry or in a health information management roleWorking knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol reviewWorking knowledge of clinical research, Food and Drug Administration
車艷鑫
沙特阿拉伯項(xiàng)目安全主管，英語(yǔ)流利聽(tīng)說(shuō)讀寫，有海外工作經(jīng)歷優(yōu)先，配合項(xiàng)目安全總監(jiān)進(jìn)行項(xiàng)目安全管理
林懿翀
美容師為顧客提供皮膚護(hù)理、美容美體服務(wù)； 職位要求：有美容院工作管理經(jīng)驗(yàn)形象好，氣質(zhì)佳，有溝通理解能力強(qiáng)、有服務(wù)意識(shí)；具有親和力和團(tuán)隊(duì)精神，有上進(jìn)心
按照操作要求進(jìn)行分揀，裝箱，包裝。要求年齡18-50歲，身體健康吃苦耐勞，無(wú)傳染病。包吃包住。聯(lián)系電話微信15221362790
楊經(jīng)理
1、智能語(yǔ)音AI質(zhì)檢專員
【工作內(nèi)容】主要負(fù)責(zé)外呼問(wèn)卷、AI 業(yè)務(wù)的線上、線下質(zhì)檢工作
【人員要求】需熟練操作電腦，專業(yè)不限
【質(zhì)檢班次】早9晚6，每周休息兩天（不一定周六日休息），綜合薪資3200-4500
2、質(zhì)檢專員
【工作內(nèi)容】錄音質(zhì)檢、質(zhì)控等工作
【人員要求】不限學(xué)歷，需熟練操作電腦
【質(zhì)檢班次】早9晚6，每周休息兩天（不一定周六日休息），綜合薪資3000-4000
3、客服專員（不含銷售）
【工作內(nèi)容】客服中心工作，公司穩(wěn)定辦公條件好，不外出、不加班、不含銷售成分（電話回訪為運(yùn)營(yíng)商及其他政企機(jī)構(gòu)做服務(wù)質(zhì)量的滿意度調(diào)研）免費(fèi)培訓(xùn)有無(wú)經(jīng)驗(yàn)均可。
【人員要求】踏實(shí)穩(wěn)定、普通話標(biāo)準(zhǔn)
【全職班次】早9晚6，六日雙休法定節(jié)假日休，綜合薪資3200-4500
【半全職班次】早9晚4，六日雙休法定節(jié)假日休，綜合薪資2200-3000 地址：燕郊漢王路漢王制造人工智能產(chǎn)業(yè)園綜合樓二層（天洋廣場(chǎng)附近，公交305、306）
華通順泰
崗位職責(zé)： 1、完成所負(fù)責(zé)項(xiàng)目財(cái)務(wù)日常管理工作，組織項(xiàng)目財(cái)務(wù)核算、報(bào)表填報(bào)、成本控制、預(yù)算管理、資金管控、納稅申報(bào)、風(fēng)險(xiǎn)管理、審計(jì)對(duì)接等相關(guān)工作； 2、負(fù)責(zé)與銀行的對(duì)接，負(fù)責(zé)銀行授信的管理、保函、信用證等辦理； 3、負(fù)責(zé)項(xiàng)目會(huì)計(jì)分析報(bào)表及分析報(bào)告的編制及審核工作； 4、負(fù)責(zé)對(duì)項(xiàng)目預(yù)算執(zhí)行情況分析，并匯報(bào)給項(xiàng)目管理團(tuán)隊(duì)； 任職資格： 1、工作年限：5年以上工作經(jīng)驗(yàn) 2、行業(yè)、項(xiàng)目經(jīng)驗(yàn)：有海外工作經(jīng)驗(yàn)優(yōu)先、有工程行業(yè)經(jīng)驗(yàn)優(yōu)先 3、能力、性格特質(zhì)：踏實(shí)細(xì)心、善于溝通、熟練使用office辦公軟件 4、教育背景：大學(xué)本科以上 5、語(yǔ)言能力：英語(yǔ)四級(jí)，聽(tīng)說(shuō)讀寫熟練，能獨(dú)立對(duì)外交流 6、性別與年齡：不限 7、其他：中共黨員優(yōu)先，注會(huì)、中級(jí)會(huì)計(jì)師優(yōu)先5、負(fù)責(zé)合同財(cái)稅條款的審核，負(fù)責(zé)項(xiàng)目合規(guī)審核及風(fēng)控管理工作。
林懿翀
崗位職責(zé)： 1、完成所負(fù)責(zé)項(xiàng)目財(cái)務(wù)日常管理工作，組織項(xiàng)目財(cái)務(wù)核算、成本控制、預(yù)算管理、資金管控、風(fēng)險(xiǎn)管理、審計(jì)對(duì)接等相關(guān)工作； 2、負(fù)責(zé)項(xiàng)目會(huì)計(jì)分析報(bào)表及分析報(bào)告的編制及審核工作； 3、負(fù)責(zé)對(duì)費(fèi)用預(yù)算執(zhí)行情況分析，并匯報(bào)給財(cái)務(wù)經(jīng)理； 4、負(fù)責(zé)費(fèi)用報(bào)銷、日常付款等日常工作。 任職資格： 1、工作年限：2年以上工作經(jīng)驗(yàn) 2、行業(yè)、項(xiàng)目經(jīng)驗(yàn)：有海外工作經(jīng)驗(yàn)優(yōu)先、有工程行業(yè)經(jīng)驗(yàn)優(yōu)先 3、能力、性格特質(zhì)：踏實(shí)細(xì)心、善于溝通、熟練使用office辦公軟件 4、教育背景：大學(xué)本科以上 5、語(yǔ)言能力：英語(yǔ)四級(jí)，聽(tīng)說(shuō)讀寫熟練 6、性別與年齡：不限 7、其他：中共黨員優(yōu)先，注會(huì)、中級(jí)會(huì)計(jì)師優(yōu)先
林懿翀
免費(fèi)求職
企業(yè)直招 不收取任何費(fèi)用
專業(yè)招聘
專人服務(wù) 入職速度快50%
優(yōu)質(zhì)服務(wù)
24小時(shí)客服響應(yīng) 快速解答今日招聘網(wǎng)是由濱興科技運(yùn)營(yíng)的人才網(wǎng)，未經(jīng)今日招聘網(wǎng)同意，不得轉(zhuǎn)載本網(wǎng)站之所有招工招聘信息及作品
浙公網(wǎng)安備 33010802002895號(hào) 人力資源服務(wù)許可證 330108000033號(hào) 增值電信經(jīng)營(yíng)許可證 浙B2-20080178-14 出版物經(jīng)營(yíng)許可證 新出發(fā)濱字第0235號(hào) 浙B2-20080178-14
互聯(lián)網(wǎng)違法和不良信息舉報(bào)中心：0571-87774297 donemi@163.com
下載APP
關(guān)注今日招聘微信服務(wù)號(hào)