Project Engineer

MES Engineer Level 1

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.

What we are looking for:

• 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.

About Lonza

At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.