IT - MES Engineer

SHL (Scandinavian Health Ltd) is currently the world's largest privately-owned designer, developer and manufacturer of advanced drug delivery systems. The organization was established in 1989 by Swedish entrepreneurs Roger Samuelsson and Martin Jelf with the goal of combining world-class manufacturing in Asia with the strengths of Western Management practices. SHL manufactures devices including pen injectors, auto injectors and inhaler systems. We also manufacture a range of other products including pressure mattress systems, patient lifting slings, medical soft goods, beds, neurosurgical devices, catheters and industrial equipment.

瑞健集團(SHL)成立於1989年，目標以西方管理模式在亞洲打造具有國際水準的生產中心。如今，在全球製藥及生物科技領域，SHL已成為藥物輸送系統的OEM/ODM領導製造商，如自動安全注射器。除此之外，SHL還擴展許多產品線，像是軟性結構類醫療產品、醫療氣墊床、醫療床、腦神經手術器具、工業 設備和醫療用吊昇設備等，目標市場為北美、歐洲及亞洲。

【Job Overview】

The MES Software Engineer will be an integral member of the PLM/MES team pushing technical advancement of the manufacturing execution system which is part of SHL digitalization journey. In cooperation with the business owners, the Senior MES Software Engineer will be working on the planning, assessment, proposing and implementing solutions fulfilling business requirements in MES system. Together with the PLM/MES team, the Senior MES Software Engineer is responsible for the design, implementation, testing and deployment of solutions for manufacturing process. This position will support business departments to improve operational performance and capability in our manufacturing facilities worldwide. MES軟體工程師將與使用者單位合作，負責MES的規劃、評估和技術解決方案的提出。 並與 PLM/MES 團隊一起，負責製造生產相關解決方案的設計、實施、測試和部署。 該職位的目標是支援業務部門以提高運營績效和生產力，實現和維護全球製造生產部門必要的軟體系統。

【Responsibilities】

• Align requirements with software and systems capabilities and provide feasible solutions to business owners.
• Plan, design, and implement manufacturing solution(s) incl. MES, CIM and needed integration aspects according to industry best practices to improve Overall Equipment Effectiveness of company.
• Develop and execute test cases, scripts, and protocols that sufficiently document alignment between design, implementation, and business requirements to fulfill GxP CSV (Computer System Validation) practice.
• Assist users in the correct use and consultation of responsible manufacturing software systems.
• 瞭解使用者需求與軟體系統功能，為使用者提供適切的解決方案。
• 開發、計劃和執行製造軟體系統解決方案，包括MES、CIM 和整合介面根據行業最佳解決方案，實踐支持運營績效持續改進。
• 開發和執行測試範例、腳本和協議，充分且完整記錄程式更改和業務需求之間的一致性，以符合GxP CSV (Computer System Validation) 電腦系統驗證實務。
• 協助使用者正確使用及諮詢負責的製造軟體系統。

【Qualification】

• Bachelor degree above, ideally in Computer Science, Information Technology, or related majors
• 3+ years of development experience with Siemens Opcenter/CAMSTAR technologies such as CDO, CLF, Designer, Opcenter Portal, Portal studio, modeling, MOM connect, Opcenter intelligence, or Opcenter rich client application development.
• Experience in customized integration development by using Opcenter WCF services & .NET API.
• 5+ years of experience with development languages such as .NET, C#, HTML/JSP, XML, CSS, XSL, and Microsoft SQL Server
• Knowledge and hands-on expertise in Siemens Opcenter solution portfolio is a plus.
• Knowledge of Good Manufacturing Practices (GMP), GAMP 5, computer systems validation concept, FDA 21 CFR part 11, data integrity principles and documentation standards is a plus
• Proficient in communication both oral and written, using English and Mandarin Chinese
• 大學以上學歷，資訊工程、資訊管理、計算機科學相關、資訊科學等優先。
• 3 年以上使用 Siemens Opcenter/CAMSTAR 技術（例如 CDO、CLF、Designer、Opcenter Portal、Portal studio、建模、MOM 連接、Opcenter 智能或 Opcenter 客戶端）的開發經驗者佳。
• 有使用 Opcenter WCF service或 .NET API的開發經驗者佳。
• 5 年以上使用 .NET、C#、JavaScript、HTML/JSP、XML、CSS、XSL 和 Microsoft SQL Server 的開發經驗。
• 在 Siemens Opcenter 解決方案組合方面提供紮實的知識和專業知識，將優先考慮。
• 了解良好生產規範 (GMP)、GAMP 5、計算機系統驗證概念、FDA 21 CFR 第 11 部分、數據完整性原則和文件標準，將優先考慮。
• 能熟練使用英語和中文進行口頭和書面交流。