ATS Automation Tooling Systems Inc.

Senior MES Engineer

Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Computer Science, Information Systems, or a related field.
  • 7+ years of experience in MES solutions for pharmaceutical, biotech, or life sciences manufacturing.
  • Strong knowledge of GMP regulations and data integrity principles.
  • Hands-on experience with MES platforms like Emerson Syncade or Körber PAS-X.
  • Expertise in MES configuration and integration within manufacturing operations.
  • Proven troubleshooting and analytical skills.
  • Excellent written and verbal communication skills.

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 settings.
  • Serve as a technical subject matter expert for MES platforms, aiding production and quality teams.
  • Support MES lifecycle activities from requirements gathering to operational support.
  • Lead change management efforts and controlled system updates.
  • Assist in investigations and resolution of MES-related issues.
  • Mentor and develop a team of MES engineers to establish a scalable practice.
  • Collaborate with Sales to identify new business opportunities and enhance MES solutions.

Benefits

  • Opportunities for career development and mentorship.
  • Collaborative work environment with stakeholders across production and IT.
  • Engagement in high-impact projects within a growing MES practice.
  • Support for industry-standard best practices in a regulated environment.
Full Job Description
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

About ATS Automation Tooling Systems Inc.

ATS Automation Tooling Systems Inc. is a Canadian company that designs and builds factory automation systems. The company was founded in 1978 and is headquartered in Cambridge, Ontario. ATS Automation Tooling Systems Inc. operates through four segments: Automation Systems Group, Life Sciences, Renewable Energy and IT. The company provides custom automation solutions to a variety of industries, including automotive, consumer products, electronics, energy, healthcare, and others. ATS Automation Tooling Systems Inc. has operations in North America, Europe, and Asia.
Learn more about ATS Automation Tooling Systems Inc.
Size
5,000 employees
Industry

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