醫護非視不可專區

1.護士或護理師執照 2.無透析經驗可 3.具ICU或ER或內科經驗佳，精IV。 4.具透析經驗佳。

1.血液透析中心護理人員，須輪班。 2.有護理(師)執照，具ICU、急診經驗尤佳。 3. 其它護理長交辦事項。

會害怕居服初期案量不穩定嗎? 初期案量少，初期前輩帶。 實習能賺錢，給500補貼車馬費。 相關與案家互動、表單填寫、照顧技巧 帶到您可以獨力完成相關流程。 (1) 提供長照2.0規範之居家服務內容，協助長者日常生活照顧服務，翻身拍背，身體清潔或準備餐食…等。 (2) 服務地區永康區、安南區、東區。 (3) 上班時段：日班。 (4) 薪資待遇：拆帳制，BA碼：60％(依接案及技巧)，AA碼：50％ (5) 可上班日：不限。 (6) 福利制度：依公司規定，開案獎金、不定時聚餐、提供護腰、移位帶。 (7) 需求人數：1~3人。

會害怕居服初期案量不穩定嗎? 初期案量少，初期前輩帶 前輩帶新人，機構提供新人500元/天。 相關與案家互動、表單填寫、照顧技巧 帶到您可以獨力完成相關流程。 依機構開/派案速度2~3個月薪資可達26,400元以上。 1.提供長照2.0規範之居家服務內容，協助長者日常生活照顧服務,如翻身拍背,身體清潔或準備餐食...等。 2.服務地區:仁德區、歸仁區、東區。 3.上班時段:日班/晚班。 4.薪資待遇:拆帳制，BA碼:60％(依本身接案量及技巧)、AA碼:50％ 5.可上班日:不限。 6.福利制度:依公司規定，開案獎金、不定時聚餐、提供護腰、移位帶。 7.需求人數:1~3人。

(全新開幕) 林口護理師 (薪至少35K起.福利完善.速洽劉小姐0989-340-222) 1.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 2.批價掛號等醫院行政管理、協助醫生完成診斷和分析 3.記錄病患用藥記錄和各種病徵 4.教育大眾各種醫藥常識、提供病患家屬治療建議

(全新開幕)眼科醫師(地點好.診次極彈性) 薪優福利佳.速洽劉小姐0989-340-222 1. 新北地區眼科診所誠徵眼科專科醫師 2. 地點：交通便利，捷運可到 3. 門診：極彈性，可配合醫師時間 4. 薪資：有保障薪，高於行情 5. 工作單純，不須負責管理 6. 工作氣氛融洽 7. 環境佳，新市鎮 8. 診所備停車位、醫責險、可彈性排休、有年假 ~熱情歡迎有志醫師加入 我們歡迎您 謝謝~

1.非醫療、手術、藥物之視力檢查及眼鏡處方或矯治 2.配製眼鏡或隱形眼鏡 3.提供眼鏡方面問題的諮詢

誠徵 驗光生/驗光師 (薪約3萬2千元~4萬5千元) *待遇依照經驗能力可再談.應徵請洽劉小姐0989-340-222 1.配製眼鏡或隱形眼鏡 2.提供眼鏡方面問題的諮詢 3.客戶服務、銷售眼鏡相關產品 4.非醫療、手術、藥物之視力檢查及眼鏡處方或矯治

1. 協助掛號 2. 回答病人基本詢問 3. 整理病歷 4. 發送禮物 5. 電話聯繫病人

非醫療、手術、藥物之視力檢查及眼鏡處方或矯治 配製眼鏡或隱形眼鏡 提供眼鏡方面問題的諮詢 客戶服務、銷售眼鏡相關產品

1.負責診所看診業務。 2.醫學美容相關治療及專業諮詢。 3.醫學美容儀器操作。 4. 需有專科醫師執照、可報備支援。 5.具醫學美容經驗者佳。 (可培訓微整形課程)

1.進行身體評估與健康觀察，測量並記錄生理數據 2.執行醫囑與用藥管理，協助完成必要醫療檢查 3.制定與調整護理計劃，提供適切的健康促進及衛教工作 4.協助病患復健計劃，觀察疾病徵兆並進行緊急處理 5.管理與監督照顧服務員，擬定日常照護計畫 6.負責耗材管理與環境清潔，處理日常電腦文書 7.與家屬溝通照護需求，參與團隊會議提升資訊同步

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、服藥及打點滴等等 3.居家打掃、整理環境、送洗病患衣物及代購所需用品 4.主管交辦事項

1.照顧病患、提供一般健康檢查包括協助服藥與衛生教育等護理臨床工作 2.記錄病患用藥記錄和各種病徵醫院行政管理、 3.緊急(意外傷害)應變處理、運作醫藥機器及管理治療進度和服藥情形 4.輔助與安撫病患在治療過程中所產生心理上的不適，給予病患和家屬情感上適時援助 6.急救甦醒器之使用與維護、居家及慢性呼吸照護、呼吸治療器材之使用與維護，以及高壓氧氣治療之操作與維護 7.依機構交辦事項

專業護理、口腔衛生教育、治療器械準備及消毒、醫療環境維持。 護理相關學歷，肯學習，願意溝通，對病人有耐心。 能獨當一面，醫療專業服務，具備團隊合作精神。 開心工作，助人為樂。

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.

*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

有健保，賣場經驗，奶粉尿布保健食品銷售經驗，優先入取 薪資面議，排休。享勞健保，年假，年終獎金。 符合條件者再投履歷謝謝。