What are the responsibilities and job description for the Senior Manufacturing Execution Systems (MES) Automation Engineer position at Lonza?
At Lonza, we are a global leader in life sciences, operating in diverse locations worldwide. Our approach isn’t about magic; it’s about the talented individuals who collaborate to innovate solutions that help businesses and, ultimately, people. We want you to own your career and contribute ideas—big and small—that make a difference.
Location : Portsmouth, NH Hybrid
We are seeking a Senior MES Automation Engineer who will be pivotal in creating and maintaining MES authoring standards across our Portsmouth, NH site. This role requires a commitment to innovative design and implementation of MES solutions while working independently.
Key Responsibilities :
Safety
Adhere to safety protocols and complete necessary training.
Develop a thorough understanding of manufacturing equipment and process automation systems.
Resolve equipment breakdowns and address quality issues in the manufacturing suites.
Provide Subject Matter Expert (SME) support for manufacturing and other departments on automation equipment.
Conduct troubleshooting and technical analyses on manufacturing equipment and automation systems.
Lead MES engineering efforts for the tech transfer of new processes.
Perform change request assessments to support timely lot release.
Participate in cross-functional meetings as the MES / Engineering SME.
Represent the MES team at engineering meetings and participate in audits as needed.
Projects
Plan and execute complex automation projects with significant improvements.
Develop and execute test scripts across various testing phases.
Manage change requests to ensure successful project completion.
Deviations / RCAs
Support the Quality department in deviation investigations.
Review and approve deviations as part of the MES process.
Participate in Root Cause Analyses (RCAs) representing the MES perspective.
Oversee the execution of Corrective and Preventive Actions (CAPA).
Approve action plans for non-regulatory CAPA.
Engage in quality risk assessments.
Documentation
Review and revise MES and manufacturing-related SOPs and work instructions as necessary.
Oversee MES review and approval of essential documentation.
Additionally, you may assist in interviewing for new departmental roles and mentor junior engineers in the group.
Key Requirements :
Bachelor's degree in engineering or a related field with 5-10 years of automation experience.
Experience in a GMP environment is preferred.
Exceptional communication and leadership skills.
Ability to analyze information to identify critical issues and relationships.
Proven problem-solving capabilities in engineering contexts.
Willingness to fulfill on-call responsibilities as required.
At Lonza, your work contributes to impactful outcomes in life sciences. Join us where we honor ethical practices and create a positive environment for our people and the planet. Your challenge is to innovate and solve complex problems that enhance lives globally, and we’ll reward your efforts with a meaningful career.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability status, protected veteran status, or any other characteristic protected by law.
