醫護非視不可專區

※配合政府缺工獎勵補助方案，18個月共補助108000元。 【基本條件】 1.具照顧服務員結訓證書、長照小卡。 2. 已上完失智、身障課程20小時證書。 3.樂觀、主動積極、有責任感。 對老人活動安排季參與熱枕。 4.具有耐心、細心、愛心、同理心及團隊精神。 【工作內容】 1.協助長者日常生活照顧、身體照顧之協助(包含沐浴清潔)。 2.帶領長者參加健康促進活動。 3.機構場域之環境基本消毒及清潔。 4.協助開發個案 5.參與機構辦理相關之教育訓練以及執行其他主管交辦事項。

1. 有護理行政管理職經驗 2. 配合機構政策執行各項業務(評鑑，督考) 3. 負責單位人力配置及排班。 4. 督導護理人員及照服員正確執行護理技術及臨床完整護理 5. 溝通協調、規劃、組織能力佳 、向心力強、情緒管理佳等人格特質 6. 計畫並執行年度單位工作目標臨床教學等工作。 7. 配合機構願景與目標任務執行；帶領與培訓團隊提升服務品質 。

公司正在招募活力滿滿的護士/護理師，快來和我們一起創造健康的奇蹟吧！💪🌟 💉【工作內容】 1. 擁有全能技能！執行基本醫療護理作業，例如監測生命徵象、進行管路和傷口照護等操作，專業又安心。 2. 打造流暢就醫體驗！協助安排住民就醫，藥物管理，以及完成專業護理記錄。 3. 守護住民健康！感染管制觀念不只懂，技術更是手到擒來。 4. 銳利觀察力！抓住疾病徵兆和異常變化，評估、處置，甚至必要時迅速進行急救措施並完成記錄。 5. 協助新住民！自信展現專業，幫助新住民進行入住評估並適應新環境。 6. 一起合作更強大！需要擁有團隊合作的熱誠及精神！ 7. 喜歡學習新知？還能參與機構教育訓練，拓展專業能力，同時完成主管交付的其他事項。 8. 擁有內科經驗是很棒的加分項目哦！ 🌟 **無經驗也無所謂！我們提供培訓，讓你快速進入狀態，蓄勢待發！** 💼 準備好用你的專業技能和熱情，成為大家健康的守護者了嗎？加入我們，和溫暖的團隊共譜屬於你的護理篇章！❤️

治療或營養食譜作業之規劃與監督、營養分析 負責規劃食品及營養計畫，並且監督餐點的準備與供應 注意廚房衛生管理事項、人員管理、衛生教育 營養教育與營養推廣方案之參與、營養衛教 營養方案之規劃與協調，及食品保健方案中營養問題 與家屬溝通住民營養相關事宜 遵辦主管吩咐之業務 參加機構會議 機構評鑑相關事宜

1.藉徒手、儀器、或其他裝置，評估住民長輩體能狀況，以供物理處方 2.3.仔細記錄療程及住民的活動表現，以掌握住民的復能進展，並視實際狀況調整治療計畫 3. 團體運動活動帶領 復能計畫 4.具物理治療師執照 正常上下班，不輪班，六日休息。 需要兼職也可安排面試。

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

診所至2018年開始申請成為PGY訓練牙醫診所，至今已成功完成兩位PGY住院醫師的訓練，PGY住院醫師常詢問到病歷是否足夠，以及訓練的內容是否紮實等等，因此本院特別將PGY這兩年所需要完成的病例，加以整理，共計約100個臨床病例，內容涵蓋的根管治療、牙周病、固定假牙、審美牙科、活動假牙等等，如此本院PGY的訓練醫師，能有一個明確的準則，參考本院資深醫師的病例，不再瞎子摸象， PGY訓練儀式最需要熟悉的三大類病例：一、全人或跨科治療，二、牙周病治療，三、活動假牙治療，本院的門診在牙周病與活動假牙有相當的患者，可以提供牙周病以及活動假牙充分的病例，另外本院的患者都是他院轉診的顯微根管治療病例，這些病例也都需要進行後續的牙周手術，以及後續的美學復形等等，對於年輕醫師了解如何保存牙齒有相當大的啟發 本院也特別將歷年來住院醫師完成的病例，加以電子化有系統的整理，並整理成完整的手冊，讓後續的住院醫師有明確的學習準則。 本院的院長為顎咬合學會理事長，也身兼中部讀書會會長，因此每年都有線上讀書會做書籍與相關病例討論，一年滿滿的行程，可以了解國外最新的治療趨勢

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.到宅與機構提供居家護理服務,指導家屬或主要照顧者日常生活、慢病照顧技巧及管路照護 2.個案管理 3.主管交待事項 4.六日及國定假日休息 ＜意者請電洽劉小姐0930-130091 (早上8:00~晚上8:00) ＜具醫院或長照中心護理師4年以上或護士7年以上經驗＞ ＜面試需攜帶相關單位服務證明＞ ＜需具小客車駕照並會開車＞ ☆有勞、健保及勞退提撥

*意可直接電洽 陳小姐 (02)2427-2345 , 0933-933-197 1.執行血液透析專業技術及相關護理工作 2.照顧病患、提供一般健康檢查包括打針、協助服藥與衛生教育等護理臨床工作 3.記錄病患用藥記錄和各種病徵 4.無透析經驗可,須接受單位內專業訓練

1.診所門診: w1~~w5 門診: am8:00~12:00, pm3:00~6:00 pm6:00~9:30 w6: am8:00~12:00 下午晚上休診 w7:休 **2.上班時間1.(排班: 每周40小時) 2.(隔日上) 帶照 精IV 幼兒預防注射 會藥助 兒科診所 一年以上經驗 :

1.內外科臨床護理實務經驗至少一至二年 2.熟悉更換管路例如:鼻胃管、氣切、抽血及導尿管 3.具汽機車駕照(要有駕駛經驗) 4.具基本電腦文書處理能力

1.為病患翻身、捶背、擦拭身體、更衣、扶持上下床及散步等等 2.照顧病患飲食起居、服藥等等 3.打掃、整理環境、送洗病患衣物及代購所需用品

*須有牙科助理或牙科櫃檯經驗* 1. 接待病人，櫃檯掛號 2. 安排就診時間，編定先後次序 3. 將病歷及有關資料併案存檔和管理 4. 醫囑keyin、診所衛材管理、辦理約診手續 5. 協助主管交辦事項 6.*需支援後台及跟診*

長照機構護理人員提供專業照顧。 1. 進行身體評估與健康狀態觀察，及時識別異常情況。 2. 協助長者日常照護，包含餵食、更衣及清潔。 3. 提供用藥管理與紀錄，確保藥物準確給予。 4. 協助就醫安排與健康追蹤，促進治療進展。 5. 制定並執行個人化復健計劃，提升身心功能。 6. 執行感染管控措施，維持環境安全衛生。 7. 撰寫護理記錄與報告，準確呈現護理情況。 8. 與家屬溝通病情與照護需求，提供專業建議。