The Senior 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.

【Main 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.

【Skills and 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