1.Report sales progress and market share periodically. 2.Plan and output marketing tool. 3.Master product design schedule and conditions. 4.Fully understand company’s business and industrial characteristics, with the ability to adjust according to costumer’s need. 5.Evaluate contract (Payment Term, Production Process, Production Request, RMA) and seek departments’ assistance when needed to response client’s demand in real time. 6.Supply quotation and confirm order to ship goods on time. 7.Maintain existing clients, develop new clients and promote business.

6~10人應徵

3/12 業務專員(需出差大中華區)

邁拓企業股份有限公司

被動電子元件製造業

新北市新店區

1年以上

專科

1.客戶關係維護 , 主要以Foxconn 為Tier 1 需往返出差中華區以維護客情 2.處理各客戶端, 專案Design in 以及後續送樣/報價/ ..等前端業務性質 3.新/舊專案進度控管、協調、跟催 4.協助產品功能、規格、品質之確

0~5人應徵

5/09 通路開發業務(大中華區)

偉林電子股份有限公司

電腦及其週邊設備製造業

台北市南港區

3年以上

專科

5. 通路接洽及訂單處理、產品報價。 6. 業務推展，傳達及說明公司各項業務重大訊息、活動及產品。

0~5人應徵

5/02 【代徵新加坡Q Squared Solutions】 Senior Scientist (Flow Cytometry) 流式細胞技術科學家

美商IQVIA_艾昆緯股份有限公司

其他醫療保健服務業

新加坡

經歷不拘

大學

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Essential Functions: • Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines. • Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances. • Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel. • Prepares data analysis results for upload to LIMS system under the guidance of senior level staff. • Assists in quality investigations, deviations, and resolution. • Prepares buffers and solutions for analysis, as required. • Assists in the review and update of laboratory procedures and techniques. • Guides entry level staff on routine procedures and supports on-boarding of new staff. • Performs and document calibration and maintenance of laboratory equipment as assigned. • Performs and documents hands on training for other lab personnel in areas of proven competency as assigned. • Assists in the review and development of laboratory procedures and techniques. • Assists in the implementation of procedural changes as assigned. • Notifies inventory staff of supply shortages. • May represent lab team on cross functional projects. • Responsible for clear, accurate, and timely communications with cross functional stakeholders. • Participates in continuing education through self-study, attending training sessions and lectures and meetings. • Supports safety, quality, and 6S requirements and initiatives. • Complies with company's procedures and applicable regulatory requirements. ** Employee Benefit and Salary Structure will follow Singapore Q Squared Solutions Policy.

0~5人應徵

5/06 大中華區外派業務儲備幹部

擎雷防偽科技股份有限公司

電腦軟體服務業

新北市中和區

經歷不拘

大學

培訓期間 1. 業務訓練（6-12個月）包括產業知識、B2B一對一、一對多業務開發工作。 2. 管理訓練（6-12個月）包括團隊建立、人員的選、用、育、留、汰。 *需要能學也願意學 *需重數據邏輯推導重於感覺 *需一起思考更佳解決方案的夥

0~5人應徵

5/07 [Part Time] Management Consulting管理諮詢顧問助理

美商IQVIA _艾昆緯藥品資訊股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

專科

1. 協助資料查找、彙整和校正 2. 熟悉Excel 和 PowerPoint 操作佳 3. 其他交辦事務

6~10人應徵

5/02 Consultant, Primary Intelligence (Healthcare)

美商IQVIA _艾昆緯藥品資訊股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

大學

Major Duties Performed (Main Functions) 1.Is able to design, conduct and deliver research studies independently, with minimal support from project leader a. Serves as key point of contact for a few key projects b. Manages the process of proposal preparation and/or modifications including overall bid integrity, ensures the development client reports and presentations and deliver findings to client c. To ensure the final outputs are of high quality and meeting client’s research needs d. Recommends improvements and alternative solutions to resolve problems 2.To manage and lead a team of 2-3 mid-junior level consultants a. To outline development plans for team members and to help them grow in their current roles/ move up to the next level b. To help develop the capability of team members, via providing professional inputs to the specific projects or to identify the relevant classroom training in order to maximize the performance of a strong team as a whole c. To proactively manage the team’s workload 3.Is able to maintain good partnership with a few key clients a. To own and maintain long term partnership, with the aim to become their trusted strategic business partner b. And to generate repeat business from these clients Minimum Education, Experience, & Specialized Knowledge Required: 1.Bachelor’s degree above majored in Medical, pharmaceutical, biology, sociology, statistics or related fields 2.4~10 year experience in healthcare market research，quantitative analysis or statistics experience desirable, good at statistic tools such as SPSS、Excel for programming and statistics analysis preferable 3.Deep knowledge of market research methods, tools and techniques and excellent multiple projects Management skills; Keen on market research and consulting service for perfect results 4.Innovative, strategic thinker with an enquiring mind; excellent presentation and communication skills; result and task oriented and accountable 5.Good time management and learning ability, can deliver good results under pressure

0~5人應徵

5/07 [Part Time] 研究助理/資料分析師

美商IQVIA _艾昆緯藥品資訊股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

大學

主要負責醫院臨床資料庫研究執行並協助相關行政事宜。依照研究文件進行資料分析、結果整理、進度追蹤與報告、數據的彙整及檢誤等。 *依照案件需求外派駐點

11~30人應徵

5/07 [長期兼職]Patient Support Program專案衛教師/個案管理師

美商IQVIA _艾昆緯藥品資訊股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

大學

工作內容：執行專案之疾病與產品諮詢，例如：藥品、針劑、醫材…等，以及相關衛教服務，協助專案的各項執行且細心，其執行項目如下： 1. 具有與醫療相關人員及病患良好的溝通能力 2. 依專案需求提供病人現場、視訊或線上方式，對相關疾病與藥品(材)的衛教諮詢與指導，以及協助病患問題解決 3. 依專案需求執行個案衛教管理 4. 醫專案需求執行系統操作，例如：協助同意書之申請與核對、Adverse Event 通報、藥品或醫材的庫存確認 5. 依專案需求執行病患關懷追蹤、檢查追蹤，以及安排及通知病人回診 6. 依專案執行健保相關行政工作 7. 依專案需求執行現場教學或線上的醫藥(材)使用教學 8. 定期彙整專案報表或其他主管交辦事項

11~30人應徵

5/02 Clinical Trials Assistant (CTA)

美商IQVIA_艾昆緯股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

大學

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. - Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist(iCRS), Clinical Research Associates (CRAs)/In-house Clinical Research Associate(iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. - Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. - Assist CRS/iCRS, CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. - Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. - Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. - May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval. - May perform assigned administrative tasks to support team members with clinical trial execution.

11~30人應徵

5/02 Clinical Associate Development Program (Trainee)

美商IQVIA_艾昆緯股份有限公司

其他醫療保健服務業

台北市松山區

經歷不拘

大學

**為期三個月培訓內容，結訓後依評估結果，將由主管分配至內部合適之職缺(如 CTA, SSU, CRA) Job Profile Summary: Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. RESPONSIBILITIES: •Complete appropriate therapeutic, protocol and clinical research training to perform job duties. •Gain experience in study procedures by working with experienced clinical staff. •Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices. •Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues. •Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution. • Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements. • Under close supervision may support start-up phase. • Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.

11~30人應徵

5/02 大中華區業務主管

5/02 大中華區業務

5/03 大中華區業務主管

5/09 NB大中華區業務產品經營主管 Sales PM Manager

5/03 大中華區海外業務主管

5/09 NB 大中華區海外通路區域業務主管

5/06 【擴編】大中華區業務/銷售專員(保障底薪37000起，另加績效獎金) Sales Executive (Greater China Region)

5/06 【集團總部】大中華區業務

5/03 業務專員/T380(需派駐大中華地區)

5/06 Sales Representative(大中華區)

3/12 業務專員(需出差大中華區)

5/09 通路開發業務(大中華區)

5/02 【代徵新加坡Q Squared Solutions】 Senior Scientist (Flow Cytometry) 流式細胞技術科學家

5/06 大中華區外派業務儲備幹部

5/07 [Part Time] Management Consulting管理諮詢顧問助理

5/02 Consultant, Primary Intelligence (Healthcare)

5/07 [Part Time] 研究助理/資料分析師

5/07 [長期兼職]Patient Support Program專案衛教師/個案管理師

5/02 Clinical Trials Assistant (CTA)

5/02 Clinical Associate Development Program (Trainee)

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