
Link Group
Position: Critical Manufacturing MES (CM-MES). Responsibilities include configuring MES solutions, developing backend logic, and ensuring compliance. Requires 5-9 years' experience and skills in C#, SQL Server, and MES integration.
We are looking for experienced professionals skilled in Critical Manufacturing MES (CM-MES) to deliver end-to-end MES solutions for Discrete Manufacturing and Life Sciences environments. This role involves process modeling, system configuration, and technical development to support efficient, compliant, and fully integrated manufacturing operations.Key ResponsibilitiesConfigure and customize Critical Manufacturing MES modules, including process modeling, material, equipment, and quality configurations.Develop backend logic, APIs, and system interfaces using C#, ASP.NET MVC, Web API, and SQL Server.Design and implement integration solutions between MES and other systems such as ERP (SAP), SCADA, and automation platforms via REST, OPC UA, MQTT, Web Services.Build and maintain UI extensions for operator and supervisor interfaces using HTML, CSS, JavaScript, and JScript.Support electronic batch records (EBR/eDHR), validation documentation, and ensure compliance with GMP and FDA regulations.Participate in system testing, troubleshooting, and go-live support throughout each delivery phase.Collaborate with cross-functional teams to provide MES technical functionality and drive continuous improvement.Required Skills & ExperienceOverall Experience: 5–9 years in MES or related technical rolesPreferred Certifications:Critical Manufacturing Associate (Frontend / Backend / Modeler / Automation / Administrator)Technical Skills:CM-MES configuration and workflow modelingC#, ASP.NET MVC, Web API, SQL ServerExperience with ERP integration (SAP MES, SAP MII exposure preferred)HTML, CSS, JavaScript, JScript, PythonExperience with Power BI or other MES reporting toolsKnowledge of integration protocols: OPC UA, MQTT, SECS/GEMFamiliarity with Siemens OpCenter or other MES platforms (advantage)Domain Experience:Discrete Manufacturing / Life Sciences / Medical DevicesUnderstanding of ISA-95, GMP, and validated environments
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| Opublikowana | 3 dni temu |
| Wygasa | za 22 dni |
| Rodzaj umowy | B2B, PERMANENT |
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