「KSB_專案管理師」的相似工作

This vacancy is open for talent pool collection. We will contact you if we have proper vacancies that fit with your profile. Job Mission Represent manufacturing and act as gatekeeper from manufacturing to D&E function Add value in overall manufacturing processes such as forming, machining, joining, and assembling Job Description Contribute to the solution of faults and takes the necessary initiatives and practical decisions to ensure zero repeat Identify gaps and drive assigned process improvement projects and successful delivery Initiate and drive new procedure changes and projects Develop and maintain networks across several functional stakeholders Prioritize works and projects based on business situation Transfer knowledge and train colleagues on existing and newly introduced products Education Master degree in technical domain (e.g. electrical engineering, mechanical engineering, mechatronics) Experience 3-5 years working experience in design engineering Personal skills Show responsibility for the result of work Show proactive attitude and willing to take initiative Drive for continuous improvement Able to think outside of standard processes Able to work independently Able to co-work with different functional stakeholders Able to demonstrate leadership skills Able to work in a multi-disciplinary team within a high tech(proto) environment Able to think and act within general policies across department levels Diversity and inclusion ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that diversity and inclusion is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions.

1. Review/approve of CGMP related documents like batch production records, analytical methods, specifications, validation protocol/report, COAs, APR, etc. 2. Non-conformances investigation/troubleshooting 3. Change control handing 4. Execute internal and vendor audit 5. Host external audit and related issues (including customer audit and regulatory inspection) 6. Extra assignment

1.原料藥、製劑，協助客戶於全球新註冊案件／缺失回覆及各項註冊變更。 2.原料藥、製劑，US/EU/TW 自有藥證註冊送件及變更。 3.自有藥證Life cycle maintenance及支援其他部門法規意見諮詢。

Introduction to the job Do you like challenges and do you want to work in a fast pacing supply chain environment to support some of the biggest semiconductor companies worldwide? Are you familiar with Logistics Operations and like to managing urgent demands on a daily basis?  If this sounds like you and if you have a strong customer oriented mindset, here is your mission. Role and responsibilities For our Global Operations Center in Taiwan we are searching for Supply Chain Professionals. You fulfill the demand of our customers for spare parts and tools for their maintenance activities on some of the most complex machines in the right quantity and at the right time & cost. Time is of the essence to ensure a seamless production of our customers without interruptions on our machines. -Handling of urgent material requests from worldwide customers in a rolling 24/7 shift system with the right customer focus, while meeting all milestones related to communication and execution -Monitoring of worldwide shipments  -Ability to resolve complex issues and drive improvements to further optimize processes -Ability to support escalations and provide communication proposals for review -Constructive and reliable communication with worldwide stakeholders from all departments within ASML -This position requires shift work. Education and Experience Bachelor's Degree in related subject i.e. Supply Chain Management, Information Science, Engineering etc. preferred -Minimum 1 year of relevant experience in an international company, semiconductor industry is preferred -A tactical thinker with strong interpersonal and communication skills -Analytical thinking and ability to organize and prioritize workload Skills Working at the cutting edge of tech, you’ll always have new challenges and new problems to solve – and working together is the only way to do that. You won’t work in a silo. Instead, you’ll be part of a creative, dynamic work environment where you’ll collaborate with supportive colleagues.  There is always space for creative and unique points of view. You’ll have the flexibility and trust to choose how best to tackle tasks and solve problems. To thrive in this job, you’ll need the following skills: -Stress-resistant; act under high pressure -Flexible; willing to go the extra mile for the customer -Excellent professional communication in English, written and oral -Drive for results; does not stop until solution has been found, even when obstacles arise -Team player -Change management competencies -Convincing, pro-active and “can do” mentality -Cultural awareness -Experience with ERP system(s), SAP R/3 knowledge preferred -Ability to prioritize Diversity and inclusion ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that diversity and inclusion is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions.

1. Prepare and Submit Regulatory Documentation: Compile, review, and submit high-quality regulatory applications, such as Investigational New Drug (IND) applications, New Drug Applications (NDA), Abbreviated New Drug Application (ANDA), and Marketing Authorization Applications (MAA), to regulatory authorities. 2. Liaise with Regulatory Authorities: Act as the primary point of contact with regulatory agencies, responding to inquiries, providing additional data, negotiating requirements, and facilitating timely approvals or resolutions. 3. Monitor and Interpret Regulatory Changes: Continuously track updates in pharmaceutical regulations, policies, and industry trends, interpreting their impact and advising internal stakeholders (e.g., R&D, legal, and marketing teams) on necessary adjustments. 4. Ensure Product Compliance: Review and approve product labeling, packaging, advertising, and promotional materials to ensure alignment with regulatory requirements, including safety, efficacy, and legal standards. 5. Manage Regulatory Submissions Timeline: Oversee the preparation and submission process to meet deadlines, ensuring all documentation is accurate, complete, and submitted in accordance with agency specifications. 6. Maintain Regulatory Records: Organize, update, and archive regulatory documentation, correspondence, and approvals in a systematic manner to support audits, inspections, and future submissions. 7. Conduct Regulatory Risk Assessments: Identify potential regulatory risks or roadblocks in product development or marketing, proposing mitigation strategies to ensure compliance and project success. 8. Handle Post-Marketing Changes: Prepare and submit regulatory applications for post-marketing changes, such as updates to manufacturing processes, labeling revisions, or formulation changes, ensuring timely approval and compliance with regulatory standards.

Context The Customer Support (CS) organization is responsible for the installations, qualification, repair and maintenance of the ASML systems at customer sites and is responsible for the necessary transfer of know-how to the customer. Local site Customer Support branches perform these tasks for the customer within the specific region. Executes system Upgrade & Installations and Relocations and provides technical support for other CS activities when needed. Conducts mostly well-defined tasks, with a higher degree of independency and under limited supervision. Requirements Requires flexibilty and openess to accommodate various work settings, locations and interactions/collaborations with different colleagues. Experienced UIR Engineer with BSc degree in relevant Technical Field (Electrical Technology, Mechatronics, Mechanical Engineering, etc.) or equivalent experience. Experienced in technical industry is required and/or semiconductor industry experience prefered. Experience in using computer applications, including data analysis tools, spreadsheet, and presentation software. Responsibilities Problem analysis and approachGather all information relevant for the problem, analyze using available means, gather additional diagnostic info if needed, decide on initial approach to solve problem and execute, consult with others. Problem handovers and routingHandover problem or problem aspects to others (2nd line support), document and package all data relevant for problem resolution (e.g. pass-downs, work orders, field service reports, system problem reports, technical reports). InstallationInstall equipment at customers locations, including equipment with new features, unload components, inspect for damage, assemble, align and test. UpgradeExecute hardware installation and perform system setup/recovery for upgrade packages as well as support locally owned field swaps by working according to an up-to-date plan and following the sequence. Provide feedback during execution in order to improve cycle time and performance. ProceduresBased on arranged customer machine time window to arrange for all (possible) parts, tools, equipment and information / knowledge to be available at start of procedure, execute procedure. Process OptimizationSignal gaps and improvement opportunities and reports it to the relevant stakeholders Training / adviceExplain appropriate actions to users to correct malfunctions, train customers in use and routine maintenance of equipment, recommend changes in user procedures when needed. Knowledge build-up and transferMaintain and broaden own knowledge, shares best known methods within the work group. CoachingProvide appropriate support and assistance to less experienced engineers on first tasks. This position requires access to controlled technology, as defined in the United States Export Administration Regulations (15 C.F.R. § 730, et seq.). Qualified candidates must be legally authorized to access such controlled technology prior to beginning work. Business demands may require ASML to proceed with candidates who are immediately eligible to access controlled technology. Diversity and inclusion ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that diversity and inclusion is a driving force in the success of our company. Need to know more about applying for a job at ASML? Read our frequently asked questions.

1. 品質目標訂定、落實、監督與改進。 2. 領導並培訓品質控制團隊，提升團隊專業素養與品質意識。 3. GMP(藥品優良製造規範)、GDP (藥品優良運銷規範)文件之制定、更新、管理、記錄等相關業務。 4. 執行內部查核、接受外部查核，並依查核結果執行矯正及預防措施。 5. 規劃與建立品質檢驗和記錄系統，標準化品保系統流程。 6. 品質相關教育訓練。 7. 與利益相關方進行有效溝通協調，確保品保管理標準能被順利執行與落實。 8. 文件簽核、年度計畫跟催及管理。 9. 主管交辦事項。 歡迎加入我們，成為品保主管的一份子，共同打造高品質的藥品、保健食品及藥妝品，讓我們的產品成為消費者的信賴選擇！立即投遞履歷，期待您的到來！

1.整合全部開發專案文件 2.協助產品PO與總PM盤點執行專案KPI及WBS、執行期中期末報告相關文件撰寫、編輯 3.掌握專案進度並確保專案執行推動 4.擔任連絡窗口、協調內外資源分配(人力、時間等) 5.進行專案內容彙整並提出需求，與內外單位溝通(業務、技術、外部機關等) 6.協調專案團隊之進度 7.依不同任務協助功能單位主管PO、總專案管理經理(總PM)調度與搭配，一同統籌專案進度 8.辦理/執行/規劃專案所需活動(包含教育訓練、舉辦活動) 9.其他主管交辦事項 【薪資待遇】依照成功大學人員進用辦法支給標準辦理

Position Summary: We are seeking a detail-oriented and experienced (Senior) Legal professional to join our Legal Affairs team. This role is responsible for providing legal support across the organization, including contract management, dispute resolution, and internal legal consultation. The ideal candidate will have strong communication and negotiation skills, and be able to work both independently and collaboratively with cross-functional teams. Key Responsibilities: 1. Draft, review, and negotiate legal documents and contracts in both Chinese and English with precision and efficiency. 2. Explain clearly contractual rights, obligations, and potential legal risks to internal stakeholders. 3. Support dispute resolution processes, including participating in settlement negotiations and providing litigation assistance. 4. Manage and coordinate with external law firms on outsourced legal matters to ensure effective collaboration and outcomes. 5. Provide legal advice and conduct thorough risk assessments on a wide range of corporate legal issues. 6. Develop and deliver internal legal training sessions to promote legal awareness and compliance across all departments.

1.協助專案經理執行專案進度追蹤與資源協調。 2.負責專案資料整理、進度報表及會議簡報製作。 3.辨識與追蹤專案問題與風險，提出解決方案建議。 4.支援跨部門溝通，確保專案需求被準確傳遞。 5.參與專案流程優化與知識庫建置。

1.各案場勘查與評估(評估方式依個案而論)及規劃。 2.專案申請設計之上下包技術服務勞務契約管控。 3.契約上下包關係與跨單位窗口溝通(含公部門機關)。 4.專案成本分析、管控案件進度與相關報表資料提供和製作。 5.專案會議管理、協調與安排。 6.需配合出差案場 7.主管交辦事項

1.機種專案管理 2.成本與良率控制 3.跟催樣品進度、良率驗證 4.客戶管理 5.例行庶務執行及其他主管交辦事項

若你(妳)具有學習及積極的心態，擅於溝通協調； 喜歡在重視團隊合作的風氣下工作，歡迎你(妳)加入我們。 【你(妳)需要做的事】 1. 分析方法開發與改善。 2. 執行安定性試驗。 3. 分析方法確效。 4. 樣品檢測分析。 5. 研發部儀器確效與管控。 6. 撰寫工作相關的計畫書與報告書。 7. 其他主管交辦事項。 【你(妳)需要具有的能力】 1. 具有英文檢定相關證書 (閱讀及寫作能力佳)。 2. 實驗室相關品質系統訓練。

1.模具/機械工程或航太工程相關科系/背景。 2.熟悉模具結構或成型原理或二次加工(如印刷、噴漆...) 3.曾有模具廠或塑膠射出成型廠相關產業經驗。 4.跨部門溝通協作整合（與模具、成型、二次加工等製造部門） 5.有工作熱情、積極學習。

1. 客戶開發及專案管理、現場簡報、需求分析、報價。 2. 負責國內外專案接洽及訂單處理。 3. 專案現地勘查及案場工程進度管理。 4. 執行開發階段各項會議策劃、召集、記錄及進度跟催等工作。 5. 客戶需求彙整、處理與分析報告。 6. 客戶現場問題溝通及訴願處理。 7. 協調跨部門問題，專案現場支援及協調。 8. 需短期、長期出差(配合負責之專案現場)。 9. 其他行政事務與主管臨時交辦事項支援。 10. 具備細心、有耐性、擅長與人溝通，且能主動、積極、有市場開發的能力。

安心醫療因業務擴大徵求人才 1.門診掛號。 2.常規護理工作,抽血,生理量測。 3.協助醫師跟診流程 4.衛教患者 5. 工作待遇：內含善化特殊院區出勤加給津貼(護理師+3000) 善化中山晨安診所-門診時間： 星期一到五 早午晚診 早診：08:30-12:00 午診：15:40-17:30 晚診：17:40-19:30 (預計114年10月搬遷後，晚診時間到20:00) 目前：星期六開早診 預計114年10月搬遷後，星期日再開午晚診。 其他說明： 本院為全天班，四周變形工時，排班制(每日工時為8小時)，每四周至少休8天。

【我們的工作】 ◉ 藥品調劑，用藥諮詢 ◉ 營養品諮詢，飲食衛教 ◉ 藥品、營養品庫存管理 ◉ 管制藥品管理、調劑 【一定要有】 ◉ 藥師執照 【加分項目】 ◉ 需具藥師相關經驗者2年以上 【薪資待遇】 ◉ 74,000起，試用期後另有績效獎金(不含班別津貼) ◉ 每年均有調薪機制 【上班時間】 ◉ 09：00-17：30 ◉ 09：00-22：00 ◉ 09：30-22：30 (中間休息) ◉ 22：30-09：00 (大夜)

1.藥品、食品、化妝品開發及製劑改良 2.新產品找尋及提案 3.製程及RD異常事件調查協助 4.處方、製程、分析方法的trouble shooting 5.研發進度管理及跟催 6.原廠產品的逆向工程及專利迴避設計 7.專利研究及專利申請 8.製程放大及產線導入作業 9.RD各類文件複核 10.完成主管交辦事項

【職責關鍵任務】大家稱呼為「產品的總舵手」 1. 新品提案，從新品定位、配方設計、包裝建議，到新品上市推廣活動的規畫，為客戶打造獨一無二的產品 2. 營養保健食品ODM/OEM的專案管理與B2B行銷策略 3. 完整掌握專案內容進度，確保專案在最高品質下順利交貨 4. 提供客製化服務，建立並強化與客戶之關係 5. 跨部門溝通協調，以利開發新品之執行 【加入生展 成為全方位人才】 生展生技為國內益生菌之領導廠商，以藥廠級研發製造能力，結合博碩士及營養師團隊的資源，從事保健品專業製造，拓展保健品國際市場。 在這裡，您能對接一流的品牌客戶，幫客戶設計暢銷明星產品！ 我們重視全方位人才的養成，提供系統性新人訓練，實施導師制度(Mentoring)引導新人適應公司文化，不定時安排專業講師授課，讓夥伴不斷精進、持續學習。 生展將招募營養、食品、生科專業背景，且喜歡挑戰不同事物的產品開發人才。 還在尋找大放異彩的舞台嗎？歡迎加入生展，一起打造獨特的明星商品、引領保健品潮流！

1.承接PM kick-off新專案訊息，與專案團隊展開開發時程與工作細項。 2.負責專案從起始、規劃、執行、監控到結案的完整生命週期管理。 3.明確定義專案範疇、目標、里程碑及交付標準，制定詳細的專案計畫並控管進度。 4.有效識別專案風險，制訂與執行風險管理計畫，確保專案順利進行。 5.跨部門協調溝通，確保資源適當分配與整合，解決專案執行中的問題 。 6.定期追蹤與報告專案進度，掌控專案成本與品質，確保達成預定目標。 7.領導與指導專案團隊，培養團隊合作精神，提升團隊績效。 8.協助組織優化內部專案管理流程與制度，提供改進建議，推動持續改善。 9.主管交辦事項。