What are the responsibilities and job description for the MES Specialist position at Inteldot?
Job Summary
We are seeking a skilled MES Systems Engineer to support the implementation, configuration, and integration of Manufacturing Execution Systems (MES) within a regulated manufacturing environment. This role focuses on system connectivity, interface development, and ongoing technical support to ensure reliable and compliant operations.
Key Responsibilities
We are seeking a skilled MES Systems Engineer to support the implementation, configuration, and integration of Manufacturing Execution Systems (MES) within a regulated manufacturing environment. This role focuses on system connectivity, interface development, and ongoing technical support to ensure reliable and compliant operations.
Key Responsibilities
- Install, configure, and maintain MES applications within Windows Server environments
- Support and troubleshoot integrations between MES and enterprise/control systems, including ERP, SCADA, and PLCs
- Configure and maintain system interfaces using industrial communication technologies such as OPC UA, MQTT, REST APIs, and Web Services
- Provide Tier 2/3 technical support, including root cause analysis and issue resolution
- Execute and support interface testing, commissioning, and validation activities in alignment with GMP requirements
- Collaborate with cross-functional teams including Automation, IT, Quality, and Manufacturing
- Assist in system documentation, including configuration specifications, SOPs, and validation deliverables
- Ensure compliance with internal standards and regulatory requirements
- Bachelor’s degree in engineering, Computer Science, Information Technology, or a related field (or equivalent experience)
- Hands-on experience or familiarity with MES platforms such as PharmaSuite, Syncade, or PAS-X
- Working knowledge of industrial communication protocols (OPC UA, MQTT, REST APIs, Web Services)
- Experience with Windows Server environments and relational databases (e.g., SQL Server, Oracle, MySQL)
- Strong troubleshooting and problem-solving skills
- Experience in pharmaceutical or life sciences manufacturing environments (GMP-regulated)
- Exposure to system validation and CSV (Computer System Validation) processes
- Familiarity with ISA-95 integration concepts
- Strong communication skills and ability to work in cross-functional teams
- Bilingual (English/Spanish)
- This is a fully onsite role supporting manufacturing operations
- Candidates must be able to work in a regulated environment and adhere to safety and compliance standards