MES Specialist

Reposted Yesterday
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San Juan, PRI
In-Office
Mid level
Information Technology
The Role
The MES Specialist will implement, configure, and support Manufacturing Execution Systems in regulated environments, ensuring compliance and system integrity through technical support and collaboration with various teams.
Summary Generated by Built In

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

  • 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
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
Preferred Qualifications
  • 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) 
Additional Information
  • 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
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    The Company
    HQ: San Juan
    19 Employees
    Year Founded: 2004

    What We Do

    Inteldot offers custom turn-key systems, systems integration, MES eBR configuration and integration solutions, business intelligence and analytics and technical staffing. We have been providing the Pharmaceutical, Manufacturing and Medical Device industries with services for a variety of applications since 2004

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