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