醫護非視不可專區

長青樹居家護理所是專業提供居家護理服務的機構，主要針對需要居家醫療照護的客戶，提供高品質的健康管理與專業照護。我們的服務對象涵蓋長期臥床患者、康復療程中的病患，以及有特殊健康需求的家庭。 上班地址: 新北市五股區成泰路三段555巷111號1樓 電話：02-2642-1938 薪資：42,000-50,000元 休假：周休二日，國定假日休 上班時間：09:00—17：30 工作內容：有多元的工作可增加收入 1. 負責個案的健康評估，例如生命體徵的量測、疾病徵兆的觀察與記錄。 2. 按照醫囑提供換管服務。 3. 指導家屬進行適當的照護技能，提供健康促進與衛教諮詢。 4. 與其他醫療團隊成員保持有效溝通，協助制定和執行個人化護理計畫。 我們誠摯地邀請有熱忱及專業護理能力的您加入長青樹居家護理所。我們注重每位患者的個別需求，用心提供優質照護服務。立即投遞履歷，期待與您一起創造更健康的生活環境！

💡 尋找充滿熱忱的「物理治療師（實習可）」！ 熱愛挑戰，想改變患者生活嗎？ 這裡是讓您的專業發光發熱的舞台！🌟 🎯 加入我們，一起完成這些任務吧 1. 提供量身打造的物理治療計畫，實現患者的健康目標 2. 利用專業器材，指導患者正確操作，確保療效最大化 3. 進行患者健康評估，細心記錄並持續追蹤治療進展 4. 符合物理治療師執業法規，確保醫療行為安全、合規 5. 用專業知識清楚解釋診療過程，助患者獲得最佳復健成果 6. 定期參加專業進修，不斷提升您的專業技能與醫療見識 7. 與多方醫療人員通力合作，給患者全方位的治療支持 🌈 這份職缺特別適合有耐心、有高度責任心且追求不斷成長的你！ 如果這是你夢想中的職涯旅程，別猶豫！ 立即投遞履歷，與我們攜手為患者創造美好生活！🚀

1.陪同醫師查房整理病歷 2.病房值班 高考護理師執照、專科護理師受訓

1. Develop analytical methods, perform analytical tests, and assist the RD team in screening formulations for the NDA and ANDA drug development. 制定分析方法，進行分析測試，並協助RD團隊篩選用於NDA和ANDA藥物開發的製劑。 2. Follow laboratory SOPs and ensure GMP compliance. 遵循實驗室SOPs並確保符合GMP規範 3. Prepare technical documents and review data for the R&D projects and drug submission. 為研發專案和藥物開發準備技術文件並審查數據 4. Responsible for performing the R&D tasks and projects, such as analytical method development, method validation, formulation screening, raw material tests, finished product release, stability study, and dissolution testing.負責執行研發任務及專案，例如分析方法開發、方法確效、配方篩選，原料測試、成品放行、安定性研究和溶出度測試。 5. Use and maintain analytical instruments, GC, HPLC, UPLC,LC-MS Dissolution Tester, Titrator, Particle size analyzer, etc. Research, diagnose, troubleshoot, and identify solutions to resolve analytical instrument issues. 使用和維護分析儀器，GC，HPLC，UPLC，LC-MS溶出度測試儀，滴定儀，粒徑分析儀等。研究，診斷，故障排除和識別解決方案以解決分析儀器問題。 6. Train, lead, and supervise junior analysts in day-to-day laboratory opera

OVERALL OBJECTIVES: -Provide leadership and oversight of designated GxP Computerized Systems (that have are relevant for Lotus Pharmaceutical) and their support teams to ensure successful delivery of key objectives, as well as compliance with applicable business and regulatory requirements. -Work with teams to implement quality systems and improvements that meet local business and regulatory requirements. -Responsibilities include administration and management of the Electronic Document Management System (EDMS), Electronic Quality Management System (EQMS), Learning Management System (LMS), as well as extended support and oversight of other GxP systems. GENERAL DUTIES: -Ensure the following key areas of GxP computerized system governance are established and maintained for applicable systems -Management: Validation planning, supplier assessment, risk management -Development 1. Validation approach & deliverables – maintain current “as is” validation state 2. Configuration and design 3. Management, development, testing, and review of software 4. Data management -Operation 1. Support services, performance monitoring, incident management, security, training, user authorizations 2. CAPA, change management, updates/patches, repair activity 3. Data integrity, periodic review, backup and restore, business continuity -Quality lead on designated Computer Systems implementations, ensuring all regulatory and compliance issues are addressed and documented -Mentor staff working on GxP computer system validation -Lead and support improvement projects to solve problems, enhance system capabilities, and expand use of GxP systems to new sites and functional areas in need. -Work with relevant teams to maintain capabilities for collecting and reporting Quality data and projects, including maintaining Quality SharePoint Portals where necessary. -Participate in internal and supplier audits as requested. -Participate in improvement initiatives and programs as requested. -Stay current with GxP and industry standards QUALIFICATIONS: -Bachelor’s degree in pharmacy or life science, or higher degree, with the right combination of extensive experience and success in the pharmaceutical industry -Education in computer science, coding or programming is a benefit -Thorough knowledge of pharmaceutical industry, quality systems, computerized system validation, GAMP 5, and relevant GxP and data integrity requirements. -Experience and skills related to the operation, administration, and overall governance of GxP computer systems and software applications. -Working knowledge of help desk software/support, databases, SaaS, and analytical reporting -Strong technical background and ability to explain complex information in simple, clear terms to non-IT personnel. Ability to assess customers IT knowledge and provide appropriate support. -Proven track record of successful GxP Computer System implementations and governance. -More than 10 years’ experience in different quality related roles within the pharmaceutical industry -Good knowledge and experience in Project Management principles and techniques. -Thorough knowledge of Quality Systems and risk-based decision making. -Experience dealing directly with regulatory agencies -Experience and skills in operating across and between different national cultures. -Good command of Mandarin and English SKILLS: -Strong leadership/team management skills -Credible and confident communicator with good presentation skills (written and verbal). -Strategic thinker with the ability to influence at all levels -Strong analytical and problem-solving ability, including identifying potential solutions, recommending and implementing methods, procedures and/or techniques for resolution. -Able to work proactively and independently.

1. Review and provide the technical recommendations for CMC documentation and Common Technical Document(CTD) dossier from a regulatory perspective. 2. Interpretation and Handling the regulatory technical query’s responses that were asked by Client and Authority during the due diligence or submission deficiency phase and provide the action plan or solution and scientific justification. 3. Responsible for evaluating the registration feasibility and mapping the global registration strategy for assigned new R&D products. 4. Cooperate and teamwork with R&D, technical, and RA PM on new R&D project technical challenges and complete the dossier till product approval. 5. Responsible for regulatory registration for export products and make sure all the documents are meet the authority‘s requirements. 6. Responsible for deficiency response preparation to ensure our response meets the authority’s requirements. 7. Accurately follow the update of the registration regulation, and provide the regulation update to the team and training.

1. Evaluation of submission feasibility for in-licensed products (major) and domestically manufactured products in the APAC region (KR, TW, HK, SG, MY, TH, VN, PH, and ID) 2. Coordination of the due diligence and production of the gap list 3. Evaluation and plan of the design, the budget, and the timeline for the bioequivalence study, the bridging study, and the clinical study in KR and TW 4. Communication with the APAC regulatory teams and partner companies to resolve the submission gap in the target markets 5. Design and consolidation of the regulatory strategy of the key milestone, the submission pathway, the submission timeline, and the launch timeline in the target markets 6. To review the License and Service Agreement 7. To support new submissions in Taiwan 8. To update of the APAC regulations 9. To prepare the consultation materials 10.To provide the justification materials on the non-clinical and clinical studies for the deficiency letter 11. To compile the ACTD format from the CTD format 12. To monitor submission progress on all company‘s projects 13. To provide improvement plans 14. The other tasks 1. 協調法規相關部門與供應商評價授權產品 2. 評估產品於亞太地區註冊之可行性，準備註冊所需相關技術文件與試驗 3. 在產品開發及送件準備期間提供法規要求的指引，協助其符合國際法規 4. 即時提供註冊用產品主檔案 5. 協助提供法規更新計畫 6. 即時支援產品維護用技術文件 7. 協助擬定合理且經濟可行之註冊計畫 8. 協助執行註冊計畫

週休二日。 門診為主,不收住院,醫師不必花太多工時於住院部.可以直接在門診學習。 醫院營業時間:早上10點到晚上6點,營業時間比較短.固定週五與週日休假。 中餐由醫院提供. 醫師主要以醫療為主. 尚未考取執照,也可來學習與工作.

工作時間可以協調。也可非全天上班，一週也可只上班某些天數。只有門診，不收住院，醫師很輕鬆。 1. 進行門診診療，負責動物的一般健康檢查與診斷。 2. 執行動物疫苗接種及緊急救護等醫療處置。 3. 協助飼主進行衛教與健康管理建議，提供專業諮詢。 4. 負責配藥、用藥建議，確保正確劑量與療效。 5. 預備並協助手術操作，維護手術室規範與清潔。 6. 管理病歷與醫療記錄，確保資料準確及保密性。 7. 確保診所醫療設備正常運作，進行日常維護。 8. 參與持續教育與法規訓練，保持專業能力更新。 醫院營業時間:早上10點到晚上6點,營業時間比較短.固定週五與週日休假。 中餐由醫院提供.醫師主要以醫療為主.

1.掛號等行政工作 2.醫療護理服務 3.協助醫師其他作業 4.內外科病房的護理工作 5.檢查針劑藥物的有效期 6.教育機構內的醫療專業知識

1. 櫃檯接待 (病患關懷、掛號、電話諮詢、出納結帳等) 2. 診間助手 (動物保定、檢驗、配藥等) 3. 住院照顧 (餵藥、餵食、清理便尿等） 4. 環境維護 (院內清潔打掃等） 5. 行政管理 (耗材補充、盤點、叫貨等） 6. 具抗壓性/愛心及耐心/適當溝通能力/儀表端莊/動作俐落/態度良善/有養寵物經驗者佳

主要分為 1.病房,院內清潔 2.跟診,保定病畜及協助看診 3.親切禮貌性回答寵物衛教問題協助飼養戶動物疾病基本判斷

執行臨床護理業務 須具護理師證書 具內科病房、長照照護工作經驗佳. 諳基本文書處理 具親和力及溝通協調應對能力、細心負責 工作時段:小夜15:30~00:00/大夜00:00~08:00 夜班費-小夜$500/大夜$900

1.執行護理臨床業務與行政管理業務 2.須具護理師證書 3.具內外科臨床工作經驗3年以上 4.曾任區域級醫院或機構之單位主管為佳 5.曾任教學醫院、醫學中心之部門組長或護理長為佳 6.具基本文書處理、整合規劃與溝通

執行護理臨床照護與行政管理業務 須具護理師證書； 具行政管理經驗或組長、臨床教師訓練為佳 具內外科之工作經驗5年以上 諳基本文書處理 具整合規劃與溝通協調能力

1.護理臨床工作督導及執行。 2.護理人員教育訓練。 3.護理人員缺編派班管理。 4.工作相關統計。 5.協助與配合護理部推動各項作業與業務。 6.單位設備管理。 7.主交辦事項。

需要有執照 評鑑資料夾整理及準備 處理個案看診資料及臨床相關藥物處理 月報表的統計，及協助護理長做文書處理 協助臨床相關文書處理業務

1.緊急應變處理 2.協助個案輔導、團體及社區資源整合連結服務 3.社區服務資源之發掘、組織、運用及服務網之建構、運作 4.綜理日間照顧中心行政管理/成本/人力資源管理業務. 5.依據組織年度目標進行運作品質管理及成果報告.

需具相關結業證書，具備相關經驗 護理,營養,復健,社工科系畢業 有長照或相關工作經驗佳 歡迎電話聯繫0935-456-540預約面試！

1.記錄用藥記錄和各種病徵 2.協助打針、協助服藥與衛生教育等護理臨床工作 3.運作醫藥機器及管理治療進度和服藥情形 日常護理工作 正職兼職皆可 無經驗可，但需具工作熱忱者，願意接受培訓者優先 上班地點 板橋中山路或土城捷運站附近 在學學生可，須有護士以上證書。 請投履歷應徵，適合會主動連絡，謝謝