醫護非視不可專區

1.綜理居家服務各項業務。 2.擬定年度工作計畫、規劃安排各項教育訓練計畫。 3.機構評鑑準備及定期報表統計分析工作。 4.訂定居家服務標準作業流程、工作手冊及相關管理制度。 5.危機預防和風險管理，緊急情況處理和通報。 6.服務對象或家屬建議、申訴案件處理。 7.開展對外公共關係與參加會議。 8.服務滿意度調查及統計分析。 9.行政事務及文書處理。 10.其他上級主管交辦事宜。

1.綜理居家服務各項業務。 2.擬定年度工作計畫、規劃安排各項教育訓練計畫。 3.機構評鑑準備及定期報表統計分析工作。 4.訂定居家服務標準作業流程、工作手冊及相關管理制度。 5.危機預防和風險管理，緊急情況處理和通報。 6.服務對象或家屬建議、申訴案件處理。 7.開展對外公共關係與參加會議。 8.服務滿意度調查及統計分析。 9.行政事務及文書處理。 10.其他上級主管交辦事宜。

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

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

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

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

小夜班 護理工作 不需輪班 時薪240起 下午6點至10點 在校生可須具護士或護理師執照。 無經驗可，願意學習。歡迎北護或亞東二技學生應徵

獨立看診 發展自我專長 團隊合作 院內工作氣氛融洽

採輪班制 高考物理治療師合格 鼓勵治療師從事自費徒手，抽成高，歡迎對自費有興趣、想提升技術、發揮所長的治療師(徒手獎金不含在薪水內，獎金另算) 周一至周五上午08:30-12:30 下午14:00-18:00 晚上17:30-21:30/週休二日/週六早上(一個月大約輪2~3次)09:00-12:00有加班費 符合勞基法，見紅就休。

工作內容： 1、提供居家身體照顧服務。 2、提供長照需求者日常生活照顧服務。 3、提供長照需求者家事服務協助。 依公司規定、白天班、假日班 依長照服務需求者需求時間,與照服員可服務時間媒合。

1. 專科護理師(nurse practitioner，簡稱NP)協助執行處置、協助書寫病程記錄、協助開立醫囑等 2. 在醫師指示下協助醫師執行醫療輔助行為諸如插鼻胃管或協助開立檢查單等工作

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

1.承接衛生主管機關感控相關之業務-如手部衛生及組合式照護 2.感染管制委員會職秘 3.院內感染之監測 4.參與感染控制相關會議及執行決議事項 5.宣導院內感染衛生教育、傳染病通報及法令 6.聯絡、協調、諮詢(衛生主管機關、院內各部門科室) 7.全體員工之健康監測 8.辦理感染管制之在職教育

牙科助理職務說明： 1. 認識及操作牙科器械與設備 2. 協助醫師臨床門診 3. 有相關牙科助理經驗者優先錄取 4. 休假依照勞基法規範 5. 需輪班

1.運用中國醫學方法，藉望、聞、問、切方式配合科學新知，診察人體各部所生之疾病，分析致病之原因 2.對症處方，運用方藥、手法、物理、針灸等方法，配合使用科學儀器及藥物，為患者作整體治療 3.提供有關中醫藥方面知識的諮詢

一對一到府服務內容: 1. 協助沐浴，更衣，上下床等 2. 居家簡易打掃、整理環境，備餐食，代購生活日用品等 3.陪同復建，回診，外出，陪伴，安全看顧等 我司有配合就業服務站缺工獎勵,到職後可自行申請

★具長照小卡，失智課程20小時及身障課程20小時結訓證明★ 1.做飯煮菜，沐浴擦澡 2.居家打掃，代購用品