- 月薪38948~45624元 苗栗縣竹南鎮 工作經歷不拘 今天剛更新展開
1. 於實驗動物舍或田間畜牧場執行動物（豬隻、雞隻及齧齒類等）試驗。 2. 執行動物樣本之採集與檢測，如病原核酸、疾病抗體。 3. 執行微生物（細菌、病毒）採樣、培養分離及鑑定。 4. 執行政府計畫或廠商委託試驗檢驗，並協助結果資料彙整、分析及報告撰寫。 5. 其他主管交辦事項。 國內外大學畜牧獸醫學、動物科學、生命科學等相關系所大學(含)以上畢業。(依法進用保障名額，具原住民身分尤佳) 薪資待遇：碩士畢業45,624元、學士畢業38,948元。 （依農業部計畫標準；碩士級研究專員月薪44,000~48,000元，學士級研究專員37,000~42,000元，固定或變動薪資因個人資歷或績效而異） 經歷要求： 1. 具獸醫學背景優先。 2. 具動物實驗經驗（豬、雞及齧齒類等）者佳。 3. 具微生物操作經驗者佳。 職能條件： 1. 具實驗設計規劃、獨立執行實驗及報告撰寫能力為佳。 2. 具良好溝通協調能力為佳。 3. 具英文資料閱讀與理解能力為佳。 工作地點：苗栗縣竹南鎮科東二路52號 ※應徵期限：自即日起，擇優通知面試後，決定是否錄取。 ※應徵方式： 1.意者請將履歷自傳表等相關資料E-mail至hr@mail.atri.org.tw，主旨請註明：應徵碩士(或學士)級計畫助理-動物醫學組(動物實驗)-姓名。 2.經書面評估資格符合者，擇優通知面試，資格不符或資料不齊者，恕不另行通知或退件。 ※面談時請攜帶下列表件： 1.履歷自傳表。請檢附相關經歷與職能之摘要說明資料，以供評估。 2.國民身分證正本。 3.最高學歷證件正本。
產假產檢假良好升遷制度尾牙員工在職教育訓練 - 月薪30000~45000元 高雄市三民區 工作經歷不拘 今天剛更新展開
1. 業務相關報表、合約、標案管理及追蹤、更新。 2. 客戶訂單處理、規格確認、報價作業。 3. 一般文書資料處理及歸檔工作。 4. 協助業務對內/外連絡事宜。 5. 院方盤點表製作及結帳。 6. 主管交辦事項等內外勤工作。 7.配合公司行銷活動並隨時更新客戶以及市場競爭資訊。 ※需自備汽車，外勤性質，可獨立作業後，享有汽車津貼。
三節獎金員工團保員工結婚補助生育補助產假 - 月薪40000~50000元 雲林縣水林鄉 3年工作經驗 1天前更新展開
1. 熟悉電力系統檢修及相關維護 2. 熟悉空(含空調設備、空壓機)、水、機、消、電等五大系統 3. 協助產線設備維運與保養 4. 熟悉水電維修相關零件採購 5.協助支援產線及倉管相關工作事務
全勤獎金年終獎金員工團保免費供餐員工聚餐 - 月薪30000~50000元 屏東縣長治鄉 工作經歷不拘 今天剛更新展開
1. 協助製程方法之開發與技轉，放大設計與SOP撰寫 2. 食品原料及相關文獻之蒐集、整理與分析 3. 產線作業之規劃與管理，以提升產能，降低成本
產假員工生日禮金年終獎金績效獎金員工團保 - 月薪38000元 台南市新市區 工作經歷不拘 1天前更新展開
★專業能力 1. 熟悉微生物(細菌、病毒等)、細胞等相關實驗操作 2. 具分子生物學相關背景知識 3. 具研究抗微生物、抗癌等作用機制實務經驗 ★軟實力 1. 研究文獻、實驗資料搜集及分析 2. 工作態度積極、處事細心、勇於創新 ★加分事項 1. 會操作蛋白質純化表現優先錄取 2. 其餘主管交辦事項 ※符合上述條件再投遞履歷謝謝
全勤獎金勞保健保加班費 - 年薪900000元 台北市中山區 2年工作經驗 14天前更新展開
1.產品市場調查與分析 2. 擬定銷售計畫、執行銷售活動，傳遞產品價值，達成業績目標。 3. 執行客戶分級與建立長期的合作伙伴關係。 4. 完成產品於醫院之進用流程，保護既有市場。 5. 及時提供客戶正確詳實的產品資訊與產品知識，並迅速反應客戶的意見及市 場資訊，同時完成所需表報資料。 6. 其他主管交辦事務。
產假產檢假全勤獎金年節獎金年終獎金 - 月薪29000元 高雄市左營區 工作經歷不拘 2天前更新展開
電視.廣播與網路廣告之自有品牌. !!高額月薪絕不是夢!! 1.保障底薪+高額績效獎金(超過政府基本底薪規定) 2.二個月上手.四個月穩定.六個月達人. 3. 完整S.O.P.教育訓練培育訓練. 4.知名品牌,最高底薪+高額獎金. 5.巨蛋捷運站.交通便利. 享公司完整福利 1.週休二日,無須加班 2.上班時間AM9：00~12:00~PM13:00~17：30 午休一小時 3.享勞、健保、勞退 4.三節禮金或贈品 5.年假比照勞基法 名額有限~剩餘4名額.還在等什麼~歡迎您加入我們的行列!!!
就業保險產假產檢假安胎假全勤獎金 - 面議（經常性薪資達4萬元或以上） 台北市信義區 2年工作經驗 2天前更新展開
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
- 面議（經常性薪資達4萬元或以上） 台北市信義區 3年工作經驗 2天前更新展開
1. Plan and execute internal audits and special projects to evaluate the risks and the effectiveness of related controls. 2. Prepare reports for each engagement and communicate audit observations with corporate, regional, and local management. Apply problem solving skills to issues and provide practical and constructive recommendations. 3. Develop credibility and trust with operating functions to value-add internal controls and management. 4. Monitor changes in Company policies and procedures to align with the applicable Regulations, Standards, and industry practices.
- 面議（經常性薪資達4萬元或以上） 台北市信義區 6年工作經驗 2天前更新展開
1. Support and facilitate business user‘s requirement to seamlessly running at corporate SAP system in the landscape via analyzing, designing, and developing. 2. Work closely with the team (other SAP developers, infrastructure & system teammates) to understand business needs and deliver features in good quality at timely manner. 3. Be capable of creating and assessing software architecture/designs with multiple stakeholders. 4. Manage overall change request and/or incident backlog for the owned topics and ensure the high quality of corrections and notes for the owned topic areas and of stable assist packages with no regressions. 5. Exhibit learning agility by quickly upskilling on new tasks and concepts. 6. Assist our business users during product deployment, critical operations, and system rollout via standard infrastructure, creating maintenance notes and documentation. 7. Will be providing presentations and workshops.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 1年工作經驗 2天前更新展開
1.開發調整分析方法(HPLC, GC, IC...)，協助產品製程開發，分析方法之確校 2.執行實驗室設備3Q 3.研擬審查藥典相關產品規格及分析測試，建立藥典規格 4.操作化學分析儀器進行分析，協助產品放行
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 5年工作經驗 2天前更新展開
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.
- 面議（經常性薪資達4萬元或以上） 南投縣南投市 10年工作經驗 2天前更新展開
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.
- 月薪37000~70000元 南投縣南投市 工作經歷不拘 2天前更新展開
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
-
