Specialist - MES

Pharmagend Global Medical Services Pte Ltd; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A pharmaceutical service provider in Singapore is seeking a MES Engineer to implement and support Honeywell Manufacturing Execution System (MES). The role involves collaboration with IT, Production, and Engineering teams to ensure system compliance and optimize processes. Candidates should possess a Bachelor’s degree and at least 3 years of experience in MES implementation, preferably with Honeywell solutions. Strong technical and soft skills are essential for success in this dynamic role.

Qualifications

• 3+ years of experience in MES implementation (preferably Honeywell).
• Strong understanding of pharmaceutical manufacturing processes, automation, and IT systems.

Responsibilities

• Install, configure, and maintain Honeywell MES applications.
• Define and implement data exchange protocols (OPC, MQTT, APIs).
• Conduct functional, integration, and user acceptance testing (UAT).
• Provide technical support during go-live and hypercare phases.

Skills

Problem-solving

Analytical skills

Communication

Stakeholder management

Education

Bachelor’s degree in Engineering, Computer Science, or related field

Tools

Honeywell MES

SQL

System integration protocols

Job description

Job Summary

We are seeking a MES Engineer for implementation of Manufacturing Execution System (MES) in the pharmaceutical industry. The MES Engineer will be responsible for implementing, configuring, and supporting Honeywell Manufacturing Execution System (MES) solutions to optimize production processes, ensure data integrity, and enable real-time visibility across manufacturing operations. This role involves close collaboration with Production, IT, and Facilities & Engineering teams to deliver a robust and compliant MES environment.

The individual will be responsible for ensuring that all engineering processes and systems adhere to regulatory standards, company quality objectives, and industry best practices. This role involves supporting the development, implementation, and maintenance of quality assurance and control systems to ensure compliance with Good Manufacturing Practices (GMP), FDA, and other applicable regulations.

Key Responsibilities

System Implementation & Configuration

• Install, configure, and maintain Honeywell MES applications.
• Develop and customize workflows, recipes, and production models.
• Ensure integration with ERP, SCADA, PLC, and other plant systems.

Integration & Data Management

• Define and implement data exchange protocols (OPC, MQTT, APIs).
• Validate connectivity and real-time data flow between MES and shop-floor systems.
• Maintain data integrity and compliance with industry standards.

Testing & Validation

• Conduct functional, integration, and user acceptance testing (UAT).
• Document test results and resolve system issues promptly.

Support & Maintenance

• Provide technical support during go-live and hypercare phases.
• Monitor system performance and apply patches/upgrades.
• Troubleshoot MES-related issues and ensure minimal downtime.

Documentation & Training

• Prepare technical documentation, SOPs, and user guides.
• Conduct training sessions for operators and technical staff.

Compliance & Security

• Ensure MES system adheres to GMP, FDA, and cybersecurity standards.
• Implement role-based access control and audit trails.

Qualifications & Skills

Education

• Bachelor’s degree in Engineering, Computer Science, or related field.

Experience

• 3+ years of experience in MES implementation (preferably Honeywell).
• Strong understanding of pharmaceutical manufacturing processes, automation and IT systems.

Technical Skills

• Expertise in Honeywell MES modules (e.g., Development environment, Production Execution, Quality Management).
• Knowledge of SQL, scripting, and system integration protocols.

Soft Skills

• Excellent problem-solving and analytical skills.
• Strong communication and stakeholder management abilities.