MES Engineer (Syncade)

San Juan, Puerto Rico
Full Time
PACIV Puerto Rico
Experienced
PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is looking for an MES Support Engineer (Syncade) to provide configuration, support, and validation services for Manufacturing Execution Systems in regulated pharmaceutical manufacturing environments.

Position Responsibilities / Essential Functions:
  • Configure and maintain Syncade recipes, including version control and lifecycle management.
  • Support MES modules such as recipe authoring, workflow, equipment tracking, and material management.
  • Configure and support MES integrations with enterprise and automation systems.
  • Troubleshoot MES-related issues and support root cause analysis.
  • Support Computer System Validation (CSV) activities including test plans, scripts, and protocol execution.
  • Prepare and maintain validation documentation in compliance with GMP and data integrity standards.
  • Support change control, deviations, and CAPA activities related to MES.
  • Collaborate with cross-functional teams to ensure system functionality and compliance.
  • Participate in project meetings, design reviews, and deployment activities.
Requirements:
  • Bachelor’s degree in Computer Science, Computer Engineering, Electrical Engineering, or related technical field.
  • 5+ years of experience supporting CSV in regulated environments.
  • 3+ years of hands-on experience with MES platforms, preferably Emerson Syncade.
  • Experience with system integrations and validation in GMP environments.
  • Strong experience authoring and executing validation documentation and test protocols.
  • Strong problem-solving, communication, and documentation skills.
  • Ability to manage multiple priorities and work independently.
Desired Hard Skills:
  • Experience with Emerson Syncade MES configuration and support.
  • Knowledge of GMP, CSV, and ALCOA+ data integrity principles.
  • Experience with MES integrations with ERP or automation systems.
  • Familiarity with pharmaceutical manufacturing operations and 24/7 production environments.
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