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Lonza seeks an experienced Automation Lead to direct MES workstreams for major CAPEX projects and to shape site automation strategy. You will manage cross‑functional teams across Manufacturing, MSAT, QA and Engineering, delivering DCS/SCADA/PLC/MES solutions with strong GMP controls.
You will mentor teams, implement Lonza best practices, and ensure validation, commissioning, and turnover meet quality and safety standards at a site‑based Bend, Oregon operation.
Join Lonza's Engineering team and play a critical role in delivering cutting‑edge automation solutions across major capital projects. This is an exciting opportunity to lead the design, implementation, and deployment of automation technologies that support the manufacture of life‑changing therapies while shaping global automation standards and strategies.
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.
A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.