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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # MES Engineer Level 1 - **Company:** Lonza, Inc. - **Location:** Portsmouth, NH, United States - **Experience:** Experienced - **Contract:** Permanent contract - **Skills:** Data Analysis, Code Review, Test Scripts, Process Control Systems - **Published:** September 4, 2026 - **Apply:** https://www.dice.com/job-detail/e4e765e7-ec30-4b0f-a2c5-8e4c18fa6716 ## About the Role * Entry-level background (0?4 years) in the Pharma/Biotech industry or related cGMP manufacturing environment. * Bachelor?s degree in a STEM discipline (Science, Technology, Engineering, or Mathematics). * Strong analytical problem-solving capabilities, with the ability to evaluate engineering problems, determine cause-and-effect relationships, and propose technical solutions. * Foundational understanding of manufacturing equipment automation, process control systems, or data analysis tools (e.g., PI software). * Strong written and verbal communication skills with the ability to effectively interact with multi-disciplinary site teams. * Highly adaptable mindset with a continuous learning orientation, willingness to embrace new challenges, and a strong commitment to workplace safety and cGMP compliance. ## Description Join our team as an MES Engineer Level 1 in Portsmouth, NH, supporting the execution, testing, and troubleshooting of key Manufacturing Execution Systems (MES). This entry-level position offers hands-on experience developing process automation expertise and delivering critical solutions that support the high-quality manufacturing of life-saving medicines. This is a fully site?based role. Working together in person supports close, real?time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. 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: * Support manufacturing equipment and process automation systems, conducting root-cause analyses and troubleshooting (including PI data analysis and code reviews). * Provide Subject Matter Expert (SME) support to Manufacturing and cross-functional teams to ensure the safe and optimal operation of process automation systems in cGMP suites. * Assist with the tech transfer of new processes into the facility and evaluate change request lot assessments to support timely lot release. * Execute test scripts (design, simulation, wet testing) and manage change requests under the guidance of automation leads and supervisors. * Participate as the MES representative in deviation investigations, Root Cause Analyses (RCAs), and complete assigned CAPA action items. * Review and revise automation- and manufacturing-related SOPs, Functional Specifications, and work instructions to prevent errors and drive continuous improvement. * Collaborate closely with MES Leads, Process Scientists, and Manufacturing Supervision to deliver high-quality, compliant automation support. ## Related Videos - [More efficient software for more efficient microchips](https://www.wearedevelopers.com/videos/1164-more-efficient-software-for-more-efficient-microchips) - [Data Science in Retail](https://www.wearedevelopers.com/videos/586-data-science-in-retail) - [Are Classical Automation Frameworks Dead? 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