美時化學製藥股份有限公司

Company Introduction

750 Employees
南投縣南投市成功一路30號(南崗工業區)
Contact Person
HR Team
Phone
暫不提供
美時化學製藥成立於 1966 年,是一個立足台灣、放眼國際的學名藥廠,目前為台灣營收規模最大的製藥公司,專注生產口服癌症用藥並銷售全世界。 美時以亞洲地區最頂尖的研發中心與生產設備,也是台灣唯一同時獲得美國 FDA、歐盟 EMA、日本 PMDA、中國 FDA 及巴西 ANVISA 認證的藥廠,全力以高品質、高近用性的藥物滿足未竟的醫藥需求,改善人類生活品質,致力為病患、員工與所有利害關係人創造最大利益。 透過目前足跡廣布台灣、韓國、泰國、越南、新加坡、香港、馬來西亞、菲律賓、與中國的直營市場,以及與一線藥廠成為合作夥伴,美時的高價值產品得以銷售至世界各角落,是少數能進軍所有國際市場的台灣藥廠。

Main Products

在評估全球廣大的製藥市場與新藥開發劑型與技術後,美時看好軟膠囊型(Softgel capsules)所需的高技術門檻與高市場潛力。美時早在 2009 年前便有計畫地投資特殊劑型研發,如今已投入超過十億新台幣,2015 年即成為台灣第一個藥用軟膠囊劑型,且是唯一拿到美國藥證的藥廠,居領導地位。 美時現正在開發數項高產值及新藥軟膠囊產品,包括治療非小細胞肺癌、前列腺癌、大腸癌及腎臟癌等藥品,成功將高毒性癌症用藥與軟膠囊劑型結合,獨步亞太學名藥廠。

Benefits

■ 團隊凝聚力:一起工作,一起玩樂! 1. 美時企業日 Lotus Day 一年一度的企業日,讓我們的團隊在趣味活動中拉近距離,共創難忘回憶! 2. Yellow Friday 每月一次的Yellow Friday活動,讓您在忙碌的工作中享受輕鬆一刻,豐富多彩的活動讓團隊更緊密! 3. 部門團隊凝聚補助 我們鼓勵部門間的合作與交流,讓您的團隊關係更加緊密。 4. 社團活動:下班後的精彩延續 美食、旅行、單車等社團活動等著您參加,讓工作之餘的生活也充滿樂趣! 5. 聖誕派對 Christmas Party 聖誕派對是員工歡聚的時刻,包含表演活動和豐盛Buffet餐點,讓大家在節日氛圍中增進情誼並享受公司的關懷。 6. 多元活動 公司透過淨灘、淨山、偏鄉義診、失智關懷、弱勢捐款、公益支持等活動,善盡社會責任。 ■ 多元福利:生活無憂,未來無憂,幸福全包! 1. 優渥獎金 年終獎金、績效獎金等您來拿!只要您全力以赴,隨著公司的成長,您的努力將轉化為實實在在的獎勵! 2. 年度調薪 每年都有機會加薪升職,讓您的薪水與成就同步增長,安心迎接未來! 3. 特別休假制度 我們的特休假政策優於勞基法,讓您更好地平衡工作與生活! 4. 四節禮金、生日禮金 無論是春節、端午節、中秋節、勞動節,還是您的生日,公司準備貼心禮金,給您滿滿暖心驚喜! 5. 學習發展 從入職訓練到進階職能提升,公司提供全方位的學習環境,涵蓋自我管理、藥業專業知識、主管管理技巧等系統性學習課程,協助員工不斷成長,強化個人能力及組織競爭力。 6. 志工假 鼓勵員工參與公益活動,回饋社會。 ■ 加碼補助 結婚禮金、 住院補助、 喪葬補助、 托兒補助、旅遊津貼、 旅遊津貼、 運動津貼,關心您的生活與健康。 ■ 員工保險:全面守護您的安心 除了勞健保外,我們還提供員工團體保險,讓您在每個工作日都能放心無憂。 ■ 優於法令的健康檢查:健康第一,全面保障 我們提供每年員工身體健康檢查優於法令要求,並安排醫生駐診諮詢,及專職廠護照顧員工健康,並辦理健康講座。 ■ 美時文化:員工關懷無微不至 在美時,我們重視每一位員工,透過各種溝通管道: 員工意見調查、員工溝通大會、圓桌會議、晨會以及各式分享及討論,來了解員工的聲音與需求。國際化的多元團隊讓您在這裡感受全球職場文化的魅力。 ■ 友善的環境:工作生活兩相宜 南投廠員工餐廳免費供應多元主餐甜品水果,Twinings 茶包、咖啡機、員工休息區、溫馨哺集乳室一應俱全,讓您工作更舒適! ■ 安全與品質優先 我們重視員工安全及產品品質,提供國際認證的GMP防護服、工作鞋與防護用具等,提供安全的工作環境!

Company & Workplace

Jobs

網管人才 IT Infra Talent 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
3年以上
1. 具備問題分析能力,可有效地與使用者溝通,解決用戶端電腦周邊硬體系統問題。 2. 熟悉網際網路TCP/IP通訊協定,基本網路設備(Hub, Switch, Firewall)管理及維運。 3. 熟悉系統硬體如:伺服器主機硬體,磁碟陣列,SAN交換機安裝,規劃,管理與維運。 4. 熟悉Server作業系統(Windows 與 Linux) 安裝,規劃,管理與維護 5. 建立VM系統相關營運管理制度及備援處理程序,管理VM系統自動化及流程改善,維護相關管理文件。 6. 實體機房管理與維護,包括UPS不斷電系統,機房監控系統。 7. 管理系統維護廠商及合約簽訂事宜,規劃與執行系統年度專案與預算,與專案內外部相關工作之溝通協調。 8. 網路流量及系統效能監控、系統硬體狀態日常巡檢,建立服務告警分析、障礙排除。 9. 配合資安設備政策規劃及調整相關設定,辦理例行性系統災難復原演練事宜。 10. 其他主管交辦事項。
Full-time
Senior Level
English Required
9/27 Updated
進出口(高級)專員 Logistics (Advanced) Specialist 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
2年以上
1 Arrange shipments for all CMO products and import business related to raw materials, bulk products and finished products. 2 Provide corporate oversight of inbound and outbound shipments, including: • Carrier performance • Freight/INCO terms selection • Maintenance of appropriate documentation • Monitoring of related costs and provide budgets for related accounts • Tracking of international shipments • Ensuring necessary training and certifications are properly conducted for related functions 3 Work with internal departments as applicable in the carrier qualification process 4 Schedule orders for shipment and perform corresponding computer transactions to ship 5 Serve as point of contact for customers on any Logistics related issues 6 Responsible for providing accurate reports to track performance and enable decision making 7 Stay current with knowledge of dispatch, logistics planning, and effective supplier management 8 Other duties as assigned
Full-time
Mid to Senior Level
English Required
9/25 Updated
製程品質保證(資深)專員 OQ (Sr.)Specialist 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
1年以上
1. Facilitate Lot disposition process, reviewing GMP docs and managing timelines. 2. Support day-to-day Quality Assurance - Operations. 3. Perform batch disposition activities within specified timelines. 4. Ensure timely review of batch records, SOPs, investigations, and adherence to quality agreements. 5. Set meaningful goals, metrics for groups, and manage performance. 6. Ensure safe, quality, and timely work. 7. Participate in continuous improvement projects, including QA systems and shopfloor processes. 8. Manage non-conformances investigation and compliance. 9. Ensure quality production and operation in accordance with schedule. 10. Quality Assurance management, covering documentation control, batch record review, investigations, production support, training, and compliance initiatives.
Full-time
Mid to Senior Level
English Required
9/25 Updated
法規(資深)專員 Regulatory Affairs (Sr.) Specialist 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
經歷不拘
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.
Full-time
Entry-level
English Required
9/25 Updated
技術服務(高級)專員 Technical Service (Advanced) Specialist 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
3年以上
1. Prepare and execute process validation activities which includes development trials, troubleshooting and monitoring the process validation batches. 2. Lead cleaning development and validation activities for new products, equipment change and quality improvement. This includes preparation of change controls, cleaning development and validation documents, risk assessment, cleaning records and other associated documents as required. 3. Comply with GMP and EHS regulations 4. Other responsibility request by line manager.
Full-time
Senior Level
English Required
9/25 Updated
稅務(資深)經理 Regional Tax (Senior) Manager 美時化學製藥股份有限公司
Salary negotiable
泰國
10年以上
This position will report to Tax Director of Lotus Group and be actively involved in tax planning, compliance, controls, and reporting with focus in South East Asia. As a key contact person for tax related matters in South East Asia, He/She is expected to maintain constructive relationships with representatives from the Tax Authority and tax consultants. e/She Role & Responsibility of regional tax role: -Manage tax compliance matters including but not limited to corporate income tax, indirect tax, withholding tax, local tax, tax provisioning, and tax accounting -Review and approve the tax returns or filings prepared by local finance or external advisors and ensure tax liabilities are paid in due course; -Partner and manage the relationship with various internal stakeholders such as Controller, FP&A, and functional heads to ensure all taxes (ie. current tax, deferred tax and WHT) are properly accrued and accounted not only for monthly reporting purpose but also for forecasting/budgeting. -Manage tax queries raised by tax office to ensure they are dealt with appropriately and on timely manner. If need be, seek advice from external consultants. -Highlight any contentious tax issues and suggest any practical solutions. -Support and/or educate local financial controllers with the changes in the domestic tax regulations that are impacting their business operations. -Actively support the Group Tax Director in developing the Group’s tax strategy as the business evolved including but not limited to -Assist Tax Director of Lotus Group in implementing strategic tax decisions that drives the Group tax forward. -Identifying opportunities for further enhancement and development of the tax strategy and function. -Proactively contribute ideas that could help to mitigate tax risks and/or optimize tax opportunities for the Group. Skills and Requirements -Bachelor's degree in any Accounting Field, preferred with CPA or tax related accreditation. -Minimum 10-15 years' experience within an international tax environment, ideally in the Big 4, preferably combined with a few years of in-house experience. Strong experience with a variety of tax operations (such as indirect tax, transfer pricing & tax accounting) and ability to drive process improvements. -Proficiency in Microsoft Office applications, especially Microsoft Excel and PowerPoint, working knowledge of some ERP system is preferred. -Ability to deal with multiple stakeholders across different cultures. -Ability to work independently without much supervision.
Full-time
Executive Level
English Required
9/25 Updated
(資深)會計專員 (Sr.) Accounting Specialist 美時化學製藥股份有限公司
Salary negotiable
台北市信義區
4年以上
1.應收帳款及銷貨收入相關帳務處理 2.業務相關費用審核 3.負責月結/報表編制及分析 4.其他交辦事項
Full-time
Senior Level
English Required
9/25 Updated
(資深)品管專員(Sr.) QC Specialist 美時化學製藥股份有限公司
Salary negotiable
南投縣南投市
1年以上
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
Full-time
Mid to Senior Level
English Required
9/25 Updated
【全台營收最大上市藥廠】【獎金優渥】【冷氣廠房】【免費供餐】製造/包裝技術員 Production Operator 美時化學製藥股份有限公司
Monthly Salary NT$ 30,000~42,400
南投縣南投市
經歷不拘
※※※擴大徵才,工廠提升計畫完工,製藥產線擴大生產規模※※※ 依廠內標準作業程序和現行GMP規範,按排程和製造批次執行產品製造,工作內容包含: 1. 負責執行產品生產相關工作 2. 負責執行產品之製造 3. 負責生產進度及狀況,確實填寫批次記錄及相關表單 4. 執行設備及工作環境清潔及維護 5. 製程設備操作 (混和、打錠、造粒、充填、熔膠、壓丸、定型乾燥等)及相關GMP文件記錄填寫 6. 包裝機台操作(片裝、瓶裝、盒裝、裝箱等)及相關GMP文件記錄紀錄填寫 7. 其他主管交辦事項 加入我們的美時製藥產線團隊,讓您的技術熱情得到最大發揮! 您將獲得製藥工藝和高品質生產技術的完善訓練及升遷制度,立即加入我們,美時是您製藥成就發展之路的唯一選擇!
Full-time
Entry-level
9/25 Updated
生產專員 Manufacturing Specialist 美時化學製藥股份有限公司
Monthly Salary NT$ 28,000+
南投縣南投市
經歷不拘
Responsible for the packaging site cGMP, record, and operation compliance, and elimination of potential risks. 負責包裝現場的cGMP、紀錄、操作的合規性,以及消除潛在風險。 Periodically review and revise the GMP documents(e.g., SOP, etc.) to ensure documentation compliance. 週期性審核GMP文件(如: SOP)以確保文件與流程吻合。 Involved in the cross-function optimization project to increase the process from the quality perspective. 參與跨部門優化專案以期從品質角度提升流程。 1. Responsible for the GMP operation effectiveness on the packaging production sites. 負責包裝現場的GMP操作有效性。 2. Responsible for the site work in progress and AQL sampling following appropriate specifications. 負責現場的製程間管控(IPC)以及AQL取樣符合規範。 3. To perform the line clearance confirmation to eliminate the mix-up risks. 執行清線確認以消除混批風險。 4. To perform periodic reviews of the GMP document for the packaging, provide and proceed to the optimization proposal about the detected gaps. 執行週期性包裝部門相關GMP文件審核,針對偵測到的流程不足提案/執行優化建議。 5 To govern and enforce the cGMP processes, 5S, implemented CAPA, and quality procedures are in place and followed strictly. 監管並確保符合cGMP的流程、5S、CAPA導入、以及有品質管控的流程在線且被嚴格遵守。 6. Monitoring the OEE system and data. Periodically propose the optimization plan. 監管OEE的系統與數據。週期性提出優化建議。 7. To perform packaging-related deviation/customer complaint investigation. And carry out the related CAPA. 參與/執行包裝部門相關的偏差/客訴調查,並執行相關CAPA。 8. To provide the training of the GMP awareness to the production team. 給予製造/包裝部門提供GMP議事相關的教育訓練。 9. Carrying out the periodic Gemba walk. 執行週期性巡線。 10. To assist with the quality audit and related tasks. 支援品質稽核以及相關任務。 11. Involvement in the production operation optimization project. 參與製程優化專案。 12. Responsible for the data integrity record of the packaging team. 負責包裝部門符合數據完整性的紀錄。 13. Collaborate with departments to ensure the quality issues and documents are escalated and solved timely manner. 跨部門合作以確保品質相關文件及議題及時被呈報且解決。 14. To perform the task assigned by the supervisor. 執行主管交辦事項。
Full-time
Entry-level
English Required
9/23 Updated