南投縣南投市轉職工作機會，轉職跳槽推薦工作，提供履歷健診等強化服務|1111轉職專區-第21頁

(資深)品管專員(Sr.) QC Specialist
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資面議（經常性薪資達4萬元或以上）40000~0元
工作內容 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

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

法規(資深)專員 Regulatory Affairs (Sr.) Specialist
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資面議（經常性薪資達4萬元或以上）40000~0元
工作內容 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.

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

品質系統經(副)理 Quality Systems (Assistant) Manager
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資面議（經常性薪資達4萬元或以上）40000~0元
工作內容 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.

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

(資深)分析研究員 (Sr.) Analytical Researcher
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資月薪37000~70000元
工作內容 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

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

需求計畫(資深)專員 Demand Planning (Senior) Specialist
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資月薪37000~70000元
工作內容 1. Per Each planning cycle to organize monthly sales forecast into campaign demand plan/bulk plan for production planning team to calculate the capacity requirement, material procurement plan and form the master schedule. 2. Prepare required data, challenge, reviews to report in monthly Domestic/Export S&OP meeting; confirming market demand with CS and Marketing team in the meeting. 3. Track demand forecast and sales/B2B order progress to ensure the supply schedule meets customer requirement. 4. Track production, testing and release progress to ensure the shipment schedule is followed. 5. New product launches-Ensure that all activities are aligned and provide timely submission of net requirements and orders. 6. Trigger escalation process as necessary. Identify and address potential supply issues pro-actively. Inform sales & marketing team on the potential supply risk timely. Recording all delay root cause for each shipment. 7. As Supply planner coordinate with demand planner, who oversees domestic market product, to manage local CMO PO Placement to meet inventory requirement. SPOC, escalation to TPP representatives for domestic TW CMO. 8. Intradepartmental communication and coordination and assisting in completing work assigned by superior.

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

製造主任 Production Section Lead
企業名美時化學製藥股份有限公司
工作地點南投縣南投市
薪資月薪37000~70000元
工作內容 1. Manage manufacturing process on the shop floor, handle accident events, and report to managers. Ensure production delivery meet KPI. 2. Oversee the technicians and ensure operations follow SOP, cGMP, and EHS regulations. 3. Recruit, probation, and performance evaluation of technicians, and oversee personnel training program execution. 4. Assist SOP generation/revision and investigation of customer complaint and deviation. In responsible area, manage all equipment, instruments, and tooling. Ensure the status of equipment/devices are ready for use. 5. plan and execute assigned projects. Other works assigned by managers.

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

餐飲正職人員
供餐福利工作獎金員工聚餐
企業名麥味登南投縣府店_千沛商行
工作地點南投縣南投市
薪資月薪30000~33000元
工作內容 1、外場點餐服務、飲料製作、送餐、客席區清潔 2、內場調理區餐點製作 3、製餐前備料 4、收班清潔維護 5、物料進貨、理貨控管 6、擁有高度負責任態度 #季獎金另計

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

衛生福利部南投醫院工程約用人員面試心得
企業名衛生福利部所屬醫院
工作地點南投縣南投市
薪資月薪45000~55000元
工作內容 (一)資格：１、具國內外大專(專科)以上土木、建築相關科系畢業者或工程履約管理經驗尤佳。２、政府採購法證照者尤佳。３、具服務熱忱、溝通協調、公文寫作及熟悉office文書處理者為佳。 (二)工作內容：１、發包工程採購案規劃設計、工程及監造。２、履約管理與工程驗收相關作業。３、院內修繕業務。４、配合總務室輪調及其他臨時交辦事項。 (三)薪資+獎勵金每月約4.5萬~5.5萬

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

美工人員
企業名俊侑股份有限公司
工作地點南投縣南投市
薪資月薪31000~40000元
工作內容 1.稿件編輯設計(製稿、出片(補露白)、整合) 2.視覺設計相關知識、電腦排版設計、繪圖工具與軟體操作 3.線上看色，需與印刷師傅溝通 4.資料圖檔歸檔

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

專案管理人員
員工旅遊年終獎金員工聚餐
企業名俊侑股份有限公司
工作地點南投縣南投市
薪資月薪31000~40000元
工作內容 1.新專案項目規劃 2.專案項目進度追蹤 3.專案成本與效益確認 4.流程及系統合理化設計 5.執行主管交辦事項

查看更多

應徵

工作適配度－%

登入後即可查看

根據履歷表的填寫狀況，智慧分析您與工作的適配程度。

5/6

轉職找工作推薦

南投縣南投市轉職工作職缺結果