Syncade MES Engineer

Title:- Syncade MES Engineer

Location: Remote

Job Description: Syncade MES Engineer

Position Overview
We are seeking a Syncade MES Engineer with 1+ years of handson experience configuring, supporting, or developing within the Syncade Manufacturing Execution System. The ideal candidate has foundational Syncade skills and is ready to grow into more advanced MES development, batch design, and system integration work.

In this role, the engineer will support daytoday MES operations, implement new functionality, troubleshoot issues, and work closely with manufacturing, automation, and quality teams to ensure the system reliably supports GMP production.

Key Responsibilities

• Configure and maintain Syncade MES objects, including workflows, recipes, equipment classes, custom VBScripts, and xslt stylesheets.
• Implement approved changes, enhancements, and new functionality within the MES environment.
• Troubleshoot Syncade batch execution issues, data errors, or configuration problems.
• Support testing activities such as factory acceptance testing, integration testing, and validation (IQ/OQ/PQ)as needed.
• Collaborate with manufacturing and quality teams to gather requirements and translate them into MES changes.
• Assist with change control documentation and GMP compliance activities.
• Participate in MES deployments, upgrades, and ongoing operational support.
• Maintain accurate technical documentation for configurations and changes.

Required Skills & Experience

• 8+ years of handson experience with Syncade MES(configuration, development, or support).
• Understanding of core MES concepts such as workflows, material management, electronic batch records, and equipment modeling.
• Basic knowledge of GMP manufacturing processes and data integrity expectations.
• Ability to interpret functional requirements and convert them into technical MES configurations.
• Strong analytical and troubleshooting skills.
• Clear communication skills, including writingGMP-compliant documentation.

Preferred Qualifications

• Experience supporting manufacturing operations in pharmaceutical or biotech regulated environments.
• Familiarity with DeltaV, SQL Server databases, or integration between MES and automation systems.
• Understanding of electronic batch record design, recipe structures, and ISA88/ISA95 concepts.
• Participation in system validation or change control processes.