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MES Engineer (Syncade)

PACIV

San Juan

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Automation, Automation Systems, Biology, Change Control, Computer Engineering, Computer Science, Computer Systems, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Data Quality, Documentation, Drug Manufacturing, ERP (Enterprise Resource Planning), Electrical Engineering, GMP (Good Manufacturing Practices), Identify Issues, Manufacturing Execution Systems (MES), Manufacturing Operations, Manufacturing Systems, Materials Management, Materials Tracking, Multitasking, Problem Solving Skills, Project Design, Recipe Development, Root Cause Analysis, Source Code/Configuration Management (SCM), System Integration (SI), System Validation, Technical Support, Test Plan/Schedule, Test Scripts, Validation Documentation, Validation Testing
LOCATION
San Juan
POSTED
30+ days ago
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 productionenvironments.

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About the Company

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PACIV