轉職熱搜工作

工程師助理(洗淨液量產Post-etch) ．工作內容： 1.協助並支援實驗實行、控管及回報 2.量產作業協助 3.研究數據整理 4.實驗設備維護及保養 5.實驗室化學品廢棄物處裡及搬運 6.環境5S整理

工程師助理(洗淨液量產Post-etch) 工作內容： 1.協助並支援實驗實行、控管及回報 2.小量產作業協助 3.實驗設備維護及保養 4.實驗室化學品廢棄物處裡及搬運 重量20kg會分好幾桶 120~200kg推車要推動/一天1~2趟/推20~30公尺 ．希望背景：理工背景科系或曾經從事半導體產業經驗, 生物/化學實驗室人員 ．希望技能：Excel文書處裡 ．希望特質：細心、可配合加班 ．備註：能配合新竹、湖口支援調動者

工作內容： 1.協助並支援實驗實行、控管及回報 2.小量產作業協助 3.研究數據整理 4.實驗設備維護及保養 5.實驗室化學品廢棄物處裡及搬運 6.其他主管交辦事項

Job Distribution: -Adequately collects and manages product safety information from all applicable sources and ensures that the Global Safety Database (GSD) is used to record source information accurately, timely and completely at affiliate level. Contributes to maintaining effective oversight of local / regional / global suppliers that manage this activity permanently or temporarily. -Distributes and/or submits ICSRs to relevant destinations, as applicable. -Periodically reviews local literature, as applicable. -Distributes / submits aggregate reports such as Periodic Safety Update Reports (PSURs) to Competent Authorities (CAs) and Suspected Unexpected Serious Adverse Reaction (SUSAR) Line Listings (LLs) to Investigators, as applicable. Manages local translations and creation of annexes and cover letters where required. -Support to adequate and timely implementation of additional Risk Minimization Measures, as applicable. -Support to the Follow-up Report or Assessment for L-RMP, which is prepared in accordance with local regulatory requirements and submitted to local Health Authorities, as applicable. -Support timely and compliant management of locally required post-authorization studies, as applicable. -Contributes to effective PV business continuity arrangements and PV-related third party life-cycle management. -Contributes to PV system audits, inspections and management of non-conformances and Corrective Actions and Preventive Action (CAPA) plans. Qualifications: -BS Degree in pharmacy, medical, life sciences, chemistry or similar -Proficiency in English listening, speaking, and writing -Experience in a PV role -Demonstrated knowledge of EU and/or domestic PV regulations and guidelines -Relevant external pharmaceutical (professional) training with an advanced professional degree

Job Description EHS Standards & Compliance 1. Comply with all EHS protocols, including proper chemical handling and hazardous waste disposal. 2. Participate in regular EHS and 5S audits; contribute to continuous improvement initiatives. 3. Maintain and update Workplace-Specific Procedures (WSP) and Hazard Identification & Risk Assessment (HIRA) documentation. 4. Ensure proper functioning of emergency shower and eyewash stations; maintain first-aid kits. 5. Attend safety briefings and support routine safety communication (Safety Short Talk). PPE & Hazard Control 6. Maintain and update the PPE matrix to ensure all personnel have correct and up-to-date safety equipment. 7. Monitor and control blue light leakage risks in reliability testing equipment. Idle Equipment & Chemical Management 8. Coordinate disposal or donation of idle equipment (e.g., Display KYIII project). 9. Conduct idle chemical cleanup before new projects or per site SDR (Scheduled Disposal Request). 10. Ensure chemical SDS (Safety Data Sheets) are up-to-date and compliant with KYIII site policies. Facility Upgrades & Safety Projects 11. Support improvement of the lab air exhaust system (note: tested in May 2025, current system shows minimal function). 12. Assist with access control setup and safety door installations. 13. Replace shelving units with floor-mounted angle steel racks to enhance stability and safety. Responsible Care (RC) & Safety Actions 14. Assist with RC Code 0 and RC Code 3 action plan kickoff and implementation. 15. Handle material-related ISSUE tickets and follow up on warehouse resolution processes. Sample Preparation & Testing 1. Assist in the preparation of formulations (compounding) and pre-processing for extrusion of lighting and display materials. 2. Perform sample preparation tasks, including cutting, lamination, and hot pressing. 3. Operate integrating sphere and other optical instruments to measure brightness, color temperature, CRI, and related data. 4. Support reliability testing (e.g., high temperature/humidity, thermal cycling, aging); monitor and record test results. Data & Inventory Management 5. Maintain accurate experimental records, sample labeling, and basic data entry. 6. Manage inventory of raw materials, lab samples, and consumables, including stock checking and restocking. Lab Maintenance 7. Conduct daily maintenance and cleaning of lab tools and equipment, such as CCF fixtures and measurement tools. 8. Uphold 5S practices in the laboratory: maintain workspace cleanliness, tool organization, and proper labeling. Team Collaboration 9. Provide general support to lab supervisors and the R&D team on lab-related tasks and project execution. Qualification -學歷: 大學畢業 (化學系、化工系、化學相關科系) -工作經歷：1年以上工作經驗，具化工廠經驗者佳 -技能和專業知識：Office 操作軟體、化學品相關知識

【工作內容】 1.依試量產工單流程操作生產製程 2.設備日常檢查操作控制及產程監控 3.維持試量產產線日常運作及工作日誌書寫建檔管理、填寫相關表單 4.作業環境清潔維護 5.作業過程簡易故障排除 6.其它主管交辦事項 ☛派遣至 【財團法人工業技術研究院】

一、協助辦理《國語辭典簡編本 》編務工作： (一)稿件收發、彙整、清稿等相關工作。 (二)辭典系統維運及檢測相關工作。 (三)編審會議相關工作。 二、協助辦理辭典預收詞庫擴充及語法問題審議 工作。 三、協助辦理國語字辭典發展及推廣事項。

【工作內容】 1.計畫定期會議安排、會議記錄 2.協助工作月報及專案文件撰寫與彙整 3.計畫時程規劃管控、追蹤進度 4.計畫相關技術文件、產出報告紙本/電子檔管理與維護 5.協助計畫產出文件技術審查、品質審查 6.AI運用與英文翻譯 ☛派遣至 【財團法人工業技術研究院】