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# MES Interface SME

- **Company:** Lonza, Inc.
- **Location:** Portsmouth, NH, United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Laboratory Information Management Systems, Microsoft Project, Microsoft PowerPoint, System Testing, Test Scripts, Information Technology, Trackwise
- **Published:** August 27, 2026
- **Apply:** https://www.dice.com/job-detail/3cf35f80-af63-44a2-92f3-eae204856335

## About the Role

* Bachelor of Science degree in an applicable STEM field or Computer Science with relevant industry experience required.
 * 5?10 years of advanced experience in Automation, Quality Control, or Validation within a cGMP Pharma/Biotech environment.
 * Deep technical proficiency in MES and LIMS integration, along with strong knowledge of Lonza?s Computer System Validation (CSV) guidelines and SOPs.
 * Proven project management skills with the ability to lead validation streams, organize resources, and control project timelines.
 * Excellent cross-functional communication skills and proficiency with tools such as MS Project, Excel, Word, and PowerPoint.
 * Strong decision-making, problem-solving, and analytical capabilities in handling complex automated systems.

## Description

This is an office-first role based on site in Portsmouth, NH. Working together in person supports close, real-time collaboration and team alignment, enabling us to deliver our best work. You will work primarily in the office and laboratory settings, with the flexibility to work remotely for 20% of your time (one day per week).

What you will get:

 * An agile career and dynamic working culture.
 * An inclusive and ethical workplace.
 * Competitive hourly rate.

Compensation for this role will be determined by the candidate?s qualifications, skills, experience, and relevant knowledge.

What you will do:

 * Lead gLIMS?MES interface validation activities to ensure on-time delivery and full compliance of all validation documentation.
 * Collaborate with the Site Change Manager and Automation SME to update or replace local MES/LIMS SOPs in alignment with global quality standards.
 * Partner with gLIMS/MES leads, system users, and process owners to design, revise, and configure production recipes supporting system interfacing.
 * Execute and oversee test scripts (design, execution, and simulation) with guidance from validation leads and supervisors.
 * Ensure all integration, requirements gathering, and testing procedures strictly meet regulatory, cGMP, and quality standards.
 * Utilize quality systems (such as TrackWise) to manage deviations, change controls, CAPAs, and system updates.
 * Interface across cross-functional groups including Quality, Manufacturing Operations, and the global gLIMS project team.


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