「Operations Manager」的相似工作

• Regular account management activities include conference calls, presentations, negotiations, contracts, cost analysis & reduction, account status reports, shipment planning. • Forecasting and tracking key account metrics (quarterly & annually). • Achieve sales targets, business objectives and assigned tasks. • Partner with cross-functional teams on RFQ and drive to award. • Keep track and ensure the growth of each customer account. • Research, identify and develop existing customers’ production line/commodity portfolio. • Establish and maintain strong customer relationships for business sustainability.

本公司網址:http://www.zybt.com.tw 1.掌握細胞治療市場資訊、市場供需及特性。 2.協助交涉、客戶聯繫、簡報資料整理、開發市場。 3.客戶關係管理含合約等相關文件審查含內部流程作業。 4.商務段的進度管理、溝通協商以確保新案順利進行。 5.商務策略撰稿與擬定，並有效執行管理層交付的任務。 6.另計有績效獎金。 ※具備外泌體相關經歷者佳.

- 負責產品取證與國際法規申請（TFDA、FDA、CE） - 協助撰寫醫療軟體/AI產品相關法規文件 - 協助追蹤各國醫療法規與送審資料準備 - Handle certifications (TFDA, FDA, CE, etc.) - Prepare regulatory documentation for software/AI medical devices - Track global regulations and support submission

1.臨床試驗專案的主導、規劃、試驗進度追蹤管理、監督、回報及時程掌控。 2.管理臨床試驗相關費用與合約洽談、簽訂、付款、報帳、時程。 3.確保臨床試驗案符合GCP及相關各國法規。 4.領導跨部門團隊，協調與項目成員合作臨床試驗，案件執行管理等相關工作。 5.監督試驗過程與進度，確保所有步驟都符合GCP標準程序。 6.維護及協助臨床試驗相關文件記錄更新及管理，所有試驗文件檔案需整理並歸檔於部門內TMF。 7.其他臨床試驗相關之主管交辦事項。

Responsibilities: Leading strategy development and execution within disease area • Participate actively and ensure appropriate input based on strategic insight and scientific expertise in the respective Brand Teams  Demonstrate broad strategic thinking and planning by developing objectives, plans and actions that are effectively addressing our organizational strategy and customer needs: Ensure country medical activities are in line with approved medical strategies  Ensure country clinical trials and studies are delivered to agreed standards of time, quality and cost as well as an appropriate participation in international trials  Identify and follow up Post Marketing Trials and coordinate budget for own country/cluster  Manage/coordinate Disease Area medical budget for own country/cluster and liaise, as appropriate, with Finance and Purchasing  Liaise with Medical Director to manage unexpected events or issues such as the early close of a study at country level  Build country/cluster reputation and visibility of medical team at the international level by managing the timely execution of trials and other medical activities  Proactively provide scientific support to Commercial, Regulatory, Market Access, Outcomes Research, Pharmacovigilance and Legal Counsel • Coordinate the medical plan processes for the Disease Area in alignment with the appropriate local/cluster functions (including Commercial, Regulatory, Market Access, PV and Outcomes Research) and with the appropriate international Medical Teams (WW/EMAC/IC) Requirements: Preferred Experience & Knowledge • Extensive experience working in cross-functional teams • Extensive experience in designing and managing clinical trials across different phases of development and resolving clinical trial-related issues • Track record in effectively managing risk and compliance • Building strong relationships with External Experts within DA • Experience in developing medical plans aligned with overall disease & product objectives • Experience in developing, reporting and analyzing medical metrics • Demonstrated ability to build a team and develop a high performing organization (inclusive coaching and mentoring) Of advantage: • Knowledge and understanding of BMS Policies and Procedures • Knowledge of statistical methods • Solid track record in writing quality scientific publications and representing BMS at international congresses • Knowledge of Disease Area and local health care system/market dynamics • Understanding of environmental and industry trends and their impact on the business • Understanding of product-specific pricing issues and required contribution to pricing and reimbursement dossiers

We are seeking a Clinical Operations Coordinator to oversee the planning and execution of clinical studies in compliance with GCP/ICH guidelines and company SOPs. This role serves as the primary contact for clinical trial operations and manages day-to-day activities to ensure successful study completion. 1.. Study Oversight & Compliance - Lead planning, execution, and management of clinical studies. - Ensure compliance with GCP/ICH guidelines, applicable regulations, and company SOPs. - Act as the primary point of contact for all clinical trial operational activities. 2.. Team Leadership & Coordination - Manage day-to-day activities of the clinical operations team. - Provide guidance and oversight to ensure timelines, budgets, resources, and quality standards are met. 3.. Cross-Functional Collaboration - Work closely with clinical project managers, medical monitors, pharmacokinetics, data management, regulatory affairs, and pharmacovigilance teams. - Ensure efficient and effective study conduct through cross-functional alignment. 4.. Stakeholder Communication - Communicate study progress to internal and external stakeholders. - Identify and mitigate study risks and issues proactively. 5.. Site & Vendor Management - Oversee investigational sites and third-party vendors to ensure high-quality execution. 6.. Documentation & Systems - Ensure clinical project-related documents and systems are developed and maintained to high standards.

加入我們，推動 AI 基因產品創新，改變精準醫療的未來 我們是一家專注於 AI 基因定序與醫療影像分析 的創新科技公司，致力於運用人工智慧解析基因數據，推動精準醫療與遺傳疾病診斷的革新。我們正在尋找 基因產品專案經理，協助規劃並推動基因分析產品的研發與落地，連結生物資訊、AI 技術與市場需求，打造具影響力的創新產品。 我們的團隊秉持 開放、協作、創新 的精神，鼓勵跨領域人才融合基因科學、AI 技術與產品策略，挑戰現有框架，推動基因科技的普及與應用。你將與生物學家、研發團隊、數據科學家及市場專家密切合作，共同規劃、執行並優化 AI 基因產品，確保技術能真正改變臨床決策與生物醫學研究。 主要職責 - 基因產品專案經理 作為 基因產品專案經理，你的核心任務是連結技術與市場，確保 AI 基因產品的開發方向符合醫療與科研需求，並推動產品落地與商業化。你將需要結合 TSO 500 與 Illumina 等生物實驗技術的理解，規劃基因數據分析產品，並管理跨部門協作，確保研發與市場策略的對齊。 你的核心職責包括： - 基因產品規劃與開發：制定產品策略，確保 AI 基因分析技術符合臨床、科研與市場需求 - 數據分析與應用場景設計：與研發團隊合作，將 DNA 基因數據轉化為有價值的臨床與科研應用 - 技術與商業需求整合：串聯生物學家、工程師、醫療機構，確保產品設計符合專業與市場需求 - 市場競爭分析與定位：研究基因定序技術趨勢，制定產品優勢與市場策略 - 產品落地與技術轉化：確保 AI 基因分析技術能在醫療機構或生物研究領域順利應用 - 跨部門協作與溝通：與 AI 研發、數據科學、醫學專家團隊密切協作，確保技術可落地運行 必備技能與條件 - 具備基因定序、TSO 500、Illumina 技術相關背景，了解基因數據分析的流程與應用場景 - 熟悉 AI 與數據分析技術，具備將基因數據轉化為產品應用的能力 - 擁有產品管理或專案管理經驗，具備 2 年以上相關產品規劃與執行經驗 - 良好的市場分析能力，能規劃基因產品競爭策略與定位 - 強大的跨部門溝通能力，能與技術、商業、醫療團隊合作，推動產品落地 - 熟悉醫療與生物科技領域，理解市場需求與臨床應用場景 - 問題解決與決策能力，能在不確定性中推動產品創新與技術落地 如果你熱衷於推動 AI 在基因科學與精準醫療的應用，並希望將技術轉化為真正影響世界的產品，歡迎加入我們的團隊！ 讓我們一起結合 AI 技術與生物醫學，打造下一代基因分析產品，推動精準醫療的革新！

This position is accountable for developing shipping solutions and ensuring service quality for expansion in global markets, including the focused markets in the Canada, Europe, UK, Australia, the US, and Asian countries. The manager aims at developing new competitive shipping solutions, implementing effective shipping processes, forging strong partnerships with suppliers, and guaranteeing seamless service delivery across operations. 1. Engage in strategic commercial negotiations with multiple service providers to design and implement effective logistics solutions tailored to the unique requirements of global markets 2. Conduct in-depth analysis of new logistics solutions' competitiveness and SLA commitments, comparing them with market benchmarks, such as price competitiveness, and door-to-door shipping lead time. 3. Lead the development and successful launch of new competitive logistics solutions in global markets, including Express services with couriers and Standard services with end-to-end fully-tracked solutions. 4. Ensure that all SOPs are comprehensive, user-friendly, and aligned with operational standards. 5. Monitor the performance of each logistics and shipping service closely, utilizing data-driven insights to identify trends and areas for improvement, including INR, EDD and ADD performance. 6. Implement alternative solutions as needed to address performance gaps and ensure continuous service enhancement. 7. Make clear, proactive and effective communication with internal cross-functional teams and external users, and address any concerns promptly.

1. 生體可用率/生體相等性試驗(BA/BE)規劃執行與專案管理 2. 臨床/臨床前試驗與檢體分析(PK/ADA)專案管理 3. 協調整合試驗團隊成員與外部協同合作單位之進度 4. 主導專案起始/規畫/執行/監控/結案分析並進行風險管控 5. 依目標需求控管試驗品質/時程/成本 6. 試驗委託單位聯繫與合約時程經費掌握 7. 主管交辦事項

1.審視所屬產品線之內外部競爭環境，訂定全產品線年度業績標及策略，所訂定之目標需符合公司預算標準。所設計之行銷計畫須與GM的業務目標一致並經公司管理層檢視及同意。 2.注重高績效文化，以客戶為導向，以數據分析為基礎，推廣有效創新行銷策略，發展市場，並對結果負責。 3.維持與重要意見領的脈絡關係，經常性拜訪重點客戶，以確保行銷策略方向正確。經營相關學會及病友會，確保行銷策略之綜效。 4.與原廠(Chiesi/TaiMed)alliance、commercial team 及medical team維持正面且密切的合作以確保落地行銷策略與全球一致，已對公司有利的方式支持產品順利上市。 5.與公司內部各部門(BD、GOB、RA、Market Access、Medical、finance、HR)協作確保溝通無礙，產品查驗登記及健保策略之設定，並依審查過程可能遇到的挑戰提供必要協助，確保上市流程順暢。

Key Accountabilities: ‒ Demonstrate high standards of BMS behaviors: Integrity, Innovation, Urgency, Passion, Accountability, Inclusion ‒ Delivers results in line with product/business plan and company goals. ‒ Develop comprehensive product plan to interpret complicated marketplace, product status, and customer & patient insights. Generates strategic imperatives and competitive tactics. ‒ Leads marketing programs timely across all functions, and ensures those programs can meet strategic goals and align with product messages. ‒ Analyze complex marketplace issues through market research data and collect competitor intelligences to develop clear understanding of both internal and external environment. ‒ Be knowledgeable on cancer disease, treatment, medical terms and clinical trials. Keep observing new competitors, treatments development and industry updates. ‒ Establishes strong relationship with thought leaders and relevant societies to ensure the endorsement of products and company. Knowledge / Experience / Language ‒ Ability to connect with cross-functional colleagues and with external stakeholders. ‒ Understanding the operational model of a multinational pharmaceutical company. ‒ Able to learn disease knowledge and product knowledge very quick. ‒ Demonstrated ability to develop marketing plan independently and implement marketing initiatives timely through working with cross function. ‒ Demonstrated ability to use creative and effective ways to execute marketing projects, especially in problem solving. ‒ Demonstrated ability to effectively communicate with individuals and external within and outside the company. ‒ Demonstrated ability to work with various audiences at multiple levels and culturally diverse to deliver business expectation. ‒ Minimal of 2 years marketing experiences in pharmaceutical industry. Marketing experiences in Oncology products is preferable. ‒ Demonstrated good interpersonal skill and team work. ‒ Fluent in Mandarin and English written/oral communication.

請透過本公司官網正式提交您的職務申請，我們期待您的加入！ https://columbiasportswearcompany.wd5.myworkdayjobs.com/Columbia_Career_Site/job/Taipei-City-Taipei-City-Taiwan-Region/Product-Compliance-Manager_R-016887 =========================== Product Compliance Program Manager is responsible for managing Product Compliance, Chemical management program including RSL/MRSL management and wastewater management, leading company wastewater and product safety compliance standards throughout the global manufacturing base, with the goal to meet customer requirements, reduce/eliminate risk to workers and consumers, the environment, the company and brands. 【Product Compliance Program Development and Deployment 】 • Manage corporate Restricted Substance List (RSL) policy implementation and product compliance failure remediation with vendors partners and internal business partners, supplier product compliance tracking and reporting. • Manage corporate Chemical Management Policy deployment, aligning with industrial practice and meet the requirement. • Support research on sustainable chemistries or green chemistry alternative if require • Develop branded fiber process to ensure the brands meet global labelling regulation and requirements • Develop global labelling manual and work with internal stakeholders to create standard operation process • Support claims validation for wholesale account requests • Track Wastewater global regulation and industrial standard, meeting country regulation and align with industrial practices. • Lead the remediation if any Wastewater compliance failure, find out the root cause by partnering with vendors, provide leadership and make recommendation to minimize the business impact. • Assess international market program requirements and establish future process to support business growth • Advance Global Product Compliance Team goals and objectives through additional projects and cross-functional support as needed 【Supply Chain Product Compliance and Wastewater Management Performance Assessment】 • Execute the Chemical and Wastewater Management assessment tools (Higg FEM) to supply chain, driving the completion and verification rate improvement to give visibility of supply chain performance. • Manage and track factory KPI to measure compliance performance including wastewater discharge permit and support the integration with material sourcing system. • Conduct onsite factory audits for chemical management, RSL and wastewater compliance when necessary. 【Supply Chain Engagement, Training and Improvement】 • Identify and analyse the performance gap of supply chain to develop required training program, collaborating with manufacturing partners including liaison office material team and production. Provide recommendation to solve vendor's challenge during the program implementation. • Engage internal and external stakeholders building relationship with the company manufacturing partners and the industry including testing service providers, GIZ fabric and other brands • Lead vendor meeting to communicate vendor performance and make recommendation of score card improvement. • Communicate and deliver technical RSL and Wastewater training to internal and external stakeholders, acting as technical center to business partners for product compliance and wastewater requirement. • On-boarding the new hire from liaison offices and new vendors, introducing of company compliance policy and process • Manage capacity building programs by collaborating with business partner and service providers, including stakeholders' engagement, program status tracking, make recommendation of improvement, negotiate with vendors or manufacturing partners to adopt required change. This job description is not meant to be an all-inclusive list of duties and responsibilities, but constitutes a general definition of the position's scope and function in the company.

我們正在尋找具醫學美容背景的產品專員，負責醫美儀器與新產品的市場策略規劃、產品訓練與上市推動，並與國外原廠保持密切聯繫，確保產品在市場上的成功發展。 【工作內容】 1. 產品策略與上市規劃：負責醫學美容儀器、新產品或新技術的策略規劃，制定上市計畫並推動市場導入。 2. 產品訓練與教育規劃：制定內部及客戶端的產品訓練計畫，確保業務及醫療人員具備完整產品知識。 3. 已上市產品管理：監測產品市場表現，解決產品使用過程中的相關問題，確保市場穩定發展。 4. 銷售策略：制定最適銷售策略，提升市場競爭力。 5. 與國際大廠合作：與國外原廠保持緊密聯繫，確保產品技術資訊即時更新，並掌握市場趨勢。 6. 醫學研究：具備良好英文能力與專業背景，能閱讀醫學文獻，確保產品符合臨床應用需求。 7. 簡報與教育訓練：擁有良好口條與簡報能力，能規劃並執行產品相關教育訓練，提升市場認知度。 8. 跨部門協作：擅長溝通與協調，能與媒體行銷、業務團隊緊密合作，共同推動市場策略與產品銷售。 【我們希望您具備】 • 具醫學美容、醫療器材、護理、生技或相關專業背景 • 具市場行銷、產品管理或醫學美容產業經驗者尤佳 • 熟悉產品上市流程，具策略思維與市場敏感度 • 英文能力良好，能與國外原廠溝通並閱讀醫學文獻 • 邏輯清晰、口條流暢，擅長簡報與教育訓練 • 善於跨部門溝通協調，能與行銷、業務團隊緊密合作 【福利與發展機會】 醫美產業高成長領域，提供穩定發展機會 參與國際醫學美容技術交流，拓展專業視野 完整教育訓練與內部晉升機會 完善薪資與績效獎金制度 如果您對醫學美容領域懷有熱情，並希望在高成長產業中發展你的專業，歡迎加入我們，成為市場開拓的重要推手！

1.須經常性進手術室裡教導醫師和護理人員正確使用產品 2.協助北區業務進行客戶開發及既有客戶的維持 3.其他主管交辦事項

1.Leading cross-functional teams to create new medical battery AIO products from innovative concepts to design verification and creative go-to-market promotion. 2.Medical battery AIO product roadmap/specifications, marketing, go-to-market planning/strategy/execution, and life-cycle management 3.Responsible for driving internal/external HW + SW solution, and cooperate with 3rd party to build up the complete medical battery AIO series.

【工作內容】 1.醫療專案管理與執行 -負責維護並追蹤既有國內外醫療專案進度，協調內部資源（研發、製造、品保等）確保專案順利執行。 -與客戶密切溝通，釐清需求與技術細節，確保交付成果符合預期。 2.業務支援與新客戶開發 -與海外業務團隊合作，參與潛在醫療客戶的開發與提案作業。 -協助製作商業簡報與產品技術資料，提供前線銷售支持。 3.國際展會與市場拓展 -參與海外醫療展會與業界活動，負責展前準備、現場簡報與客戶接洽。 -收集市場回饋與競品情報，提出潛在市場與產品優化建議。 4.跨部門協調與問題解決 -擔任業務與技術團隊之間的橋樑，協助解決導入、售後、產品改版等問題。 -定期主持專案會議，追蹤關鍵時程與風險，確保專案進度與品質。 【需求條件】 1. 大學以上學歷，醫療工程、生物科技、國際企業、管理等相關科系尤佳。 2. 2 年以上專案管理或國際業務相關經驗。 3. 具備流利英文聽說讀寫能力，能獨立與國外客戶溝通與簡報。 4. 熟悉醫療產品開發流程，具醫療產品或電子設備經驗者尤佳。 5. 具備良好邏輯思維、溝通協調能力與責任感。 【加分條件】 1. 具第二外語（如日文、德文、西班牙文等）能力者佳。 2. 曾參與國際醫療展會（如 MEDICA、HIMSS、Arab Health 等）者佳。 3. 熟悉ISO 13485、醫療法規（CE、FDA、TFDA）流程者佳。 4. 有醫療系統整合、解決方案型銷售（Solution Sales）經驗尤佳。

We are seeking a highly motivated and results-driven Business Development Manager to lead our international expansion and platform marketing efforts. This role is critical in attracting international buyers, distributors, and exhibitors to the Healthcare+ Expo Taiwan, while also driving user growth and business opportunities through our Healthcare+ B2B platform. The ideal candidate is both strategic and execution-oriented, with strong international business development skills and a deep interest in healthcare, digital platforms, and global trade. You will play a key role in connecting Taiwan’s top medical suppliers with global buyers and creating high-value matchmaking opportunities. ▌Key Responsibilities International Business Development (Buyer-Focused): •Identify and research potential buyers, distributors, procurement platforms, and partners in target international healthcare markets. •Develop and execute outreach strategies to attract international attendees to the Taiwan Healthcare+ Expo, focusing on business matchmaking and procurement potential. •Coordinate with overseas associations, chambers, and trade offices to promote the expo and drive buyer recruitment. •Build and maintain strategic relationships with international buyers, industry leaders, and institutional partners. ▌B2B Platform & Marketing Execution: •Plan and implement marketing strategies for the Healthcare+ B2B Platform, including campaigns targeting international buyers and local suppliers. •Design and optimize the buyer’s onboarding experience, content flow, and engagement campaigns on the B2B platform. •Work with internal cross-functional teams (IT, marketing, content) to improve platform user experience and track conversion performance. Matchmaking Program Management: •Manage the scheduling, coordination, and follow-up of B2B matchmaking meetings between international buyers and Taiwanese suppliers (virtual or onsite). •Collaborate with team members to design tailored buyer programs, including meeting agendas, travel assistance, and post-meeting reports. •Track KPIs such as number of international buyers, successful meetings, follow-up interactions, and trade outcomes. ▌Qualifications •Bachelor’s degree or above •Minimum 5 years of experience in international business development, exhibition promotion, digital marketing, or B2B platforms. •Proven experience in working with international clients, partners, and/or trade organizations. •Strong verbal and written communication skills in English and Mandarin. •Familiarity with international healthcare markets or medical technology industries is a plus. •Excellent interpersonal skills, cross-cultural communication abilities, and team coordination capability. •Strong sense of ownership, strategic thinking, and a proactive mindset. ▌What We Offer •Strategic role bridging Taiwan’s healthcare industry with global business opportunities. •Exposure to international exhibitions, buyers, and trade missions. •Opportunities to lead impactful projects and interact with high-level stakeholders. •Collaborative team environment with mission-driven goals. •Competitive salary based on experience and qualifications.

1. 市場資訊收集與開發新客戶，可分析市場和產品趨勢。 2. 善於溝通協調，可與行銷、業務人員合作搭配。 3. 口條清晰，可規劃與執行內、外部教育訓練。 4. 須具備良好英文能力，可與國外原廠溝通聯繫、並且可執行英文簡報。 5. 與原廠窗口保持良好關係、不定期溝通新專案合作及報價。 6. 主管交辦專案執行。

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. A successful candidate will be expected to have a solid background in cell biology, immunology, immune cell differentiation and expansion processes, scale-up, experience working in or supporting a cGMP-regulated environment, as well as sound technical knowledge of manufacturing processes for engineered immune cell therapies. ROLE OVERVIEW You will have high internal visibility focusing on developing robust and scalable manufacturing platforms for allogeneic cell expansion and directed differentiation. You will have the opportunity to establish manufacturing platforms and guide product development through all stages of development to ensure project advancement. This role will work with analytical development and R&D team to understand and identify the general function, activity, characteristics, purity, stability, and safety of cell products. The role will identify the manufacturing flow and key process parameters and execute clinical manufacturing activities to provide the required information in IND package. He/She will utilize their technical expertise to ensure data is accurate and high quality under the GMP guiding principle. RESPONSIBILITYIES 1. Design and execute phase-appropriate process development studies identifying process parameters and appropriate ranges to be assessed for optimal experimental design of the study 2. Design and execute DP process-enabling studies including formulation, fill/finish, cryopreservation, thawing, and in-use compatibility study of candidate cell therapy product. 3. Testing new manufacturing technologies and platforms in partnership with R&D. 4. Develop robust, scalable, directed-differentiation processes platform. 5. Be responsible for preparation of protocols, reports, test methods, and SOPs. 6. Review and discuss analytical results and conclusions both orally and in writing. 7. Work in a team-based structure and interface with research and process development departments. 8. Maintain and ensure safe laboratory environment and work practices. 9. Ensure timely completion of testing and tasks as assigned. QUALIFICATIONS AND REQUIREMENTS 1. Master with 3+ yrs. or 6+ yrs. of relevant experience in industry with a focus on in immune l culture, differentiation, expansion, formulation process. 2. Knowledge of biology/immunology/biochemistry as applied in cell and gene therapy processes is required. 3. Hands-on experience with common cell therapy laboratory equipment and technology platforms (i.e. primary NK cells, iPSC-derived cell types, etc.) 4. Experience with cell culture bioreactor operations and process scale up with application to cell therapy is required. 5. Familiarity with flow cytometry assays and other cell-based characterization assays (i.e. cytokine release and cytolytic assays) is a plus. 6. Deep understanding of biologics industry process development strategies and best practices as applied from early development. 7. Demonstrated ability to work in a dynamic environment as a team player with a strong work ethic. 8. Excellent presentation skills, written and verbal. 9. Occasional weekend work may be required. 10. Understanding of GMP regulations is preferred. BEIGENE GLOBAL COMPETENCIES When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

1、負責海內外數位病理及人工智慧解決方案的規劃與執行，包含專案執行、開發及導入管理、追蹤和時程控管。 2、與業務/產品團隊合作，協助解決方案規劃、客戶提案溝通等，加速客戶端業務推進。 3、負責與數位病理及人工智慧專案相關的客戶關係維繫。 4、協助內部跨部門溝通，包含業務、產品、軟體工程、人工智慧等。 <資格要求> 1、優良的書面及口語溝通能力，英文溝通能力 (TOEIC: 900 / TOEFL:80 / IELTS: 6.5 或是其他相關證明 )。 2、大學以上生命科學、醫學、統計、心理、計算機科學等相關科系。 3、具備醫學資訊、人工智慧或軟體專案管理的經驗。 4、具備軟體系統導入經驗，含導入執行、系統整合等，以醫療相關場域之經驗尤佳。