5/01 化妝品保養品配方研發
- 使之覺醒生化科技有限公司
- 藥品／化妝品及清潔用品零售業
- 台北市松山區
- 3年以上
- 專科
公司有發展新計畫，此職位為擴編需求，部門人員分工配置完善。 【工作內容】 1.保養品護膚產品、洗卸產品之配方開發設計、研發、打樣。 2.保養品有效性、穩定性評估與測試觀察。 3.保養品量產製程評估、分析與優化。 4.熟悉化妝品管理法規及產品文件建檔作業。 5.跨部門溝通協調合作與主管交辦事項。 【必備條件】 1.需具備化粧保養品配方研發實務經驗。 【其他條件】 1.化粧品、化學、化工、生物科技相關科系畢業者。 2.能獨立進行產品研發作業者。 【額外福利】 1. 生日禮金 2. 三節禮金 3. 考核年終獎金 4. 活動獎金 5. 全勤獎金 6. 員購優惠
5/01 製程工程師 (沼氣及污水)
- 日成科技股份有限公司
- 其他電力器材製造業
- 台北市中山區
- 5年以上
- 專科
1. 參與新產品材料開發、選定、測試與試產 2. 設備規劃與製程最適化 3. 製程改善與優化，如沼氣及沼液製程分析與改善、製程條件制定、製程問題追蹤與改善 4. 製程維護、異常處理與改善及新製程開發 5. 建立、改善製程條件，並監控製程結果 6. 評估、引進、驗收新製程、技術設備及材料 7. 執行部門計畫及規劃執行更新部門內相關製程文件 本職位負責新產品開發、製程優化、量產放大及異常排除等工作，是公司製造部門不可或缺的一員，具有相當的重要性和良好的發展前景。 歡迎有興趣的候選人申請此職位，我們期待您的加入！
5/01 英文出口專利工程師(機械、化學、材料、電學)
- 聖島國際專利商標聯合事務所
- 工商顧問服務業
- 台北市松山區
- 經歷不拘
- 大學
協助國內客戶在外國取得專利保護，包括技術分析、提供客戶專利實務上的意見、撰寫英文專利說明書，以及撰寫回覆官方來函之正式文件等。
4/30 電化學材料研發工程師
- 台科鋰電池股份有限公司
- 電池製造業
- 台北市大安區
- 經歷不拘
- 大學
1. 協助實驗物料盤點管理、設備儀器操作 2.負責新材料的評估、測試、分析與選擇。 3. 實驗數據彙整分析
4/30 Product Compliance Manager
- 台北市中山區
- 10年以上
- 大學
The 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 deployment and Wastewater Program development 】 -Track Wastewater global regulation and industrial standard, meeting country regulation and align with industrial practices. -Develop and deploy the Wastewater Management program including policy establishment, internal business partner and vendor partner engagement and vendor training. -Develop and monitor Wastewater compliance testing program to meet country regulation and validate wastewater to ensure company taking the due diligence liability. -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 -Manage corporate Restricted Substance List (RSL) policy implementation and product compliance failure remediation with vendors partners and internal business partner, supplier product compliance tracking and reporting. -Manage corporate Chemical Management Policy deployment, aligning with industrial practice and meet the minimal requirement. -Support research on sustainable chemistries or green chemistry alternative if require 【Supply Chain Product Compliance and Wastewater Management Performance Assessment】 -Execute the 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 Wastewater 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 centre 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 wastewater 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. Columbia Sportswear Company and our portfolio of brands, including Columbia, SOREL, Mountain Hardwear and prAna, know a thing or two about adventures. After all, we've been on one since 1938, working to perfect the art of enjoying the outdoors. Behind everything we make is an employee who's found that the greatest adventure starts with joining a company that strives to do the right thing. 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.
4/30 製程工業 專案經理/專案工程師-工作地點:台北/台中/高雄 (4800)
- TUV_台灣德國萊因技術監護顧問股份有限公司
- 檢測技術服務
- 台北市松山區
- 3年以上
- 大學
1. 執行煉油石化廠資產完整性管理(AIM)及設備完整性(MI)管理技術諮詢專案的靜態設備風險評估(關鍵設篩選、腐蝕環路分析、RBI分析、IOW完整性操作視窗評估) 引導員、NDT檢測報告審查、腐蝕狀態監測報告彙整、適用性評估、SOP制訂、教育訓練講師、變更管理審查、製程安全事故調查、符合性稽核、現場輔導等技術顧問服務工作。 2. 執行轉機設備風險評估(關鍵設篩選、RBM分析) 引導員、振動頻譜分析報告審查、失效根因分析、AI故障自動診斷報告評估等技術顧問服務工作。 3. 執行長途管線相關之風險評估、管線檢測現場監驗、壓力試驗監驗、陰極防蝕驗證、開挖驗證、管線安全管理系統驗證等技術服務工作。 4. 領導並協調參與專案之業主及承攬商之相關事務及會議。 5. 監督下包廠商工作成果。
4/30 研究員
- 因華生技製藥股份有限公司
- 其他醫療保健服務業
- 台北市內湖區
- 2年以上
- 博士
1. Expertise in oral formulations development. 2. Experience in all aspects CMC includung formulation design, manufacturing process development, regulatory and quality. 3. Work experience of at least 2 years.
4/30 材料／生命科學 工程產品經理
- 法德利科技股份有限公司
- 電腦軟體服務業
- 台北市內湖區
- 1年以上
- 碩士
一、職務內容： 【材料科學產品人員】 1. 對現有客戶進行售後服務，包括產品教學、問題諮詢、障礙排除等。 2. 接受客戶委託，進行材料科學分析或新材料開發研究，包括文獻查找、研究流程設計、實驗執行、結果報告等。 3. 對潛在客戶進行產品介紹、演示、以及問題解答。 4. 協助經營產品銷售及市場分析，擬定銷售策略。 5. 其他主管交辦事項完成。 【必要技能】 1. 熟悉分子模擬計算之理論與研發流程，包含量子力學、分子力學與計算化學，具實際模擬研發經驗尤佳。 2. 具材料開發研發經驗。 【加分項目】 1. 具有使用材料科學模擬或化學資訊軟體(如Materials Studio、CASTEP、Gaussian、VASP、Schrodinger等)進行研究之經驗 2. 有專案管理與執行經驗或教學經驗 3. 有基本程式設計之經驗與概念，或熟悉任何程式語言 3. 喜愛並能願意學習、掌握各種新技術的重點 4. 有彈性、樂於接受領導、能溝通、樂於助人、習慣團隊合作
4/30 專案報告工程師 Engineer （化學 )
- 台北市北投區
- 1年以上
- 專科
1.產品測試評估報價 2.專案執行 3.客戶詢價/法規/技術回覆 4.國際環保/化學法規更新確認 5.處理部門交辦事項
4/30 【紡織材料工程師 】Material Quality Engineer – Fabric
- 台北市中山區
- 7年以上
- 大學
• Oversee, manage and coordinate all aspects of fabric quality within Amer Sports brands, T1 and T2 • Make sure all quality and delivery requirements are met. • Participate in MD seasonal development review process to drive prevention initiatives. • Be familiar with and clearly define materials quality, and policy expectations for vendors as required. • To monitor all quality aspects of material during the development and production processes. • Clearly communicate and document all concerns and potential problems. Inspect fabric or fabric process to identify the cause of errors or other problems or defects. • Visiting fabric mills to trouble shoot and ensure that there are no problems with bulk. • Educate, train and certify Suppliers factory Auditor Process; decertify as required. Initiate and follow up with corrective action plan as required. • Promoting material quality achievement and performance improvement across the organization, setting up and maintaining controls and documentation; • Collating and analyze performance data and charts against defined parameters. • Manage suppliers quality performance: Maintain Amer Sports initiatives at suppliers’ level. Analyze Supplier Quality Performance information; establish timely Root Cause analysis and Corrective Action. • Train and certify Suppliers materials personnel on Material 4 points inspection process and requirement. • Maintain the accuracy of data. Communicate and collaborate with respective parties on negative materials quality performance trend; be familiar with same Vendor’s performance indicators. • Communicate with and initiatives to develop Prevention Systems to include Process Capability Analysis, Process Improvement, Critical Quality Specifications etc.
4/30 化學合成研發工程師
- 華上生技醫藥股份有限公司
- 生化科技研發業
- 台北市南港區
- 1年以上
- 碩士
1.熟悉小分子藥物合成及設計。 2.純化分析定量實驗。 3.具有機合成經驗。 4.有抗腫瘤藥物開發相關經驗 5.實驗室與行政庶務工作執行。 6.主管交辦事項。
4/30 數據視覺化工程師－B10B
- 精誠資訊股份有限公司
- 電腦系統整合服務業
- 台北市中正區
- 2年以上
- 大學
1. 負責數據視覺化(Data Visualization)與商業智慧(BI)分析工作，開發交互式的數據視覺化儀表，提供直觀和易懂的數據展示和分析報告 2. 與數據中台或數據倉儲人員協同設計和實現數據提取、轉換和加載(ETL/CDC)工作，確保數據的準確性和完整性 3. 研究和應用新的數據視覺化技術和方法論，不斷提升數據視覺化的效果並改善用戶體驗 4. 與業務和技術團隊緊密合作，理解業務需求，設計合適的可視化解決方案 5. 提供數據分析和視覺化等呈現方面的建議和支持，幫助數據分析與業務人員進行業務決策，從而更容易發現數據特徵
4/30 RPA自動化工程師(24011101)
- 叡揚資訊股份有限公司
- 電腦軟體服務業
- 台北市中山區
- 經歷不拘
- 專科
我們的任務： 學習並了解世界最頂級的超自動化(Hyperautomation)軟體平台(包含如:RPA(機器人流程自動化)、低程式開發平台 (LCAP_Low-Code Application Platform)、AI 人工智慧等自動化科技)，幫助企業加速並優化營運流程。 我們的願景： 1. 企業加速並優化營運流程最不可或缺的夥伴與最值得信任的專業團隊 2. 共同成長，互相扶持，開放溝通，有歸屬感的幸福團隊 我們的期許： 1. 當責：視部門及團隊目標為己任，目標導向 2. 時間管理大師：在任務與當責的前提下，自己管理自己的時間，讓同仁可保留部分工作彈性。 3. 良好英文能力：與原廠的書信往來是日常，閱讀原廠的文件也是日常，若有需要也可以跟原廠直接電話溝通(您不需要有TOEIC高分, 也不需要有正確的文法，只要能夠讓原廠能夠正確了解您的問題與狀況，且能夠正確地把原廠教的解決方案 解決客戶問題 即可) 4. 加分用的特殊技術能力： RPA, VB, C#, OCR, VBA, Python, API, Hyper-V, SAAS任何相關經驗 流程梳理、流程優化、流程設計的任何管理經驗 流程自動化的軟體開發的相關經驗 問題解決&排除的能力 您，主要負責產品可以是，世界最頂級的RPA平台 更多詳情, 可以Google 關鍵字：gartner RPA magic quadrant 2024 如果有任何問題～歡迎隨時來信詢問 [email protected]
4/30 CMC Scientist/Manager
- 仁新醫藥股份有限公司
- 其他醫療保健服務業
- 台北市信義區
- 經歷不拘
- 碩士
We are looking for a CMC scientist/manager with excellent English communication for CMC management. General Statement: Lead the planning, evaluation, and execution of CMC strategy for all pipeline products. The position will be responsible for management of all CMC activities including but not limited to evaluation and selection of Drug Substance and Drug Product contract manufacturers, technical lead and oversight of contract manufacturing and contribution to regulatory submissions and interactions with regulatory authorities. The individual will report to VP, Pharmaceutical Sciences. Job Responsibilities: • Lead cross-functional planning of CMC strategies for early phase and late phase pipelines to ensure drug development timeline and achieve business targeted outcomes • Sourcing, evaluation/performing risk assessment and selection of Drug Substance and Drug Product contract manufacturers • Provide strong technical leadership and oversight of all CMC projects inclusive but not limited to technical transfer, formulation development, process development, analytical method development and validation at contract manufacturers to ensure cGMP compliance and regulatory requirements • Lead and oversight of manufacturing process optimization and scale-up, manufacturing of registration batches and process validation moving forward to commercialization • Ensure establishment of appropriate specifications for Drug Substance, Drug Product, intermediates, excipients and etc. • Review protocols, development reports, batch records, standard operating procedures, and other technical reports • Author and review relevant CMC sections of IND, IMPD and NDA submissions and ensure regulatory compliance