Senior MES Engineer

Job Description

Position Summary

We are seeking a Senior MES Engineer to support the expansion of our Manufacturing Execution Systems (MES) practice and provide on-site engineering support for pharmaceutical manufacturing operations in the RTP area, including.

This role will serve as a technical leader, delivering MES solutions that support manufacturing efficiency, data integrity, and regulatory compliance in GMP environments.

Key Responsibilities

Provide on-site and remote MES engineering support for pharmaceutical manufacturing operations
Lead the design, configuration, and deployment of MES solutions in GMP-regulated environments
Serve as a technical subject matter expert for MES platforms, supporting production, quality, and IT stakeholders
Support MES lifecycle activities including requirements gathering, system configuration, testing, validation, deployment, and operational support
Lead or contribute to change management, impact assessments, and controlled system updates
Support investigations, root cause analysis, and issue resolution related to MES applications
Lead, mentor, and grow a team of MES engineers, providing hands-on technical guidance, career development support, and day-to-day leadership to build a strong and scalable MES practice
Drive the continued growth of the MES practice by defining standards, establishing best practices, and providing technical leadership to ensure consistent, high-quality MES solution delivery
Contribute to the growth of the MES practice through standardization, best practices, and technical leadership

Collaborate closely with Sales and Business Development to support pre-sales activities, shape MES solutions, and identify new opportunities that expand the MES practice and overall business

Additional Information

Required Qualifications

Bachelor’s degree in Engineering, Computer Science, Information Systems, or a related technical discipline
7+ years of experience supporting or implementing MES solutions in pharmaceutical, biotech, or life sciences manufacturing environments
Strong knowledge of GMP regulations, data integrity principles, and validated systems
Hands-on experience with one or more MES platforms (e.g., Emerson Syncade, Rockwell PharmaSuite, Körber PAS-X, or similar)
Experience with MES configuration, integration, and support across manufacturing operations
Strong troubleshooting, analytical, and problem-solving skills
Ability to work effectively in an on-site, client-facing role
Excellent written and verbal communication skills

Preferred Qualifications

Prior experience supporting large pharmaceutical manufacturing environments
Experience with system validation, CSV, and regulated documentation practices
Knowledge of ISA-88 / ISA-95 standards and manufacturing workflows
Experience integrating MES with ERP, automation, or data historian systems