Competitive compensation and recognition programs that reward high performance.
What you will do: Design, implement, and validate MES recipes and DeltaV control strategies that support robust and compliant biopharmaceutical manufacturing processes. Partner closely with Manufacturing, Process Development, Automation, Engineering, and Quality teams to ensure seamless system integration and operational excellence. Troubleshoot and resolve MES and DeltaV system issues, minimizing production disruptions and supporting reliable plant operations. Develop and maintain technical documentation, including specifications, work instructions, and validation records in accordance with GMP requirements. Support end users through training, technical guidance, and ongoing system expertise. Drive continuous improvement initiatives, identifying opportunities to optimize manufacturing processes, automation strategies, and system performance. Contribute to the implementation of new technologies and digital manufacturing solutions that enhance productivity, compliance, and operational efficiency.
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 value diversity and are committed to creating an inclusive environment for all employees. If you-re ready to help turn our customers- breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.
