Controls and Instrumentation Engineer

automation and control technologies within a leading biopharmaceutical manufacturing environment.An inclusive and ethical workplace where collaboration and innovation are encouraged.Compensation programs that recognize high performance.A variety of benefits dependent on role and location.The full list of our global benefits can be found here: .What you will do:Design, develop, implement, and maintain control systems and instrumentation solutions that support biopharmaceutical manufacturing processes.Configure, troubleshoot, and optimise automation systems including PLCs, Distributed Control Systems (DCS), and SCADA platforms.Develop and maintain engineering documentation, including control strategies, functional specifications, control narratives, wiring diagrams, and technical drawings.Maintain, calibrate, and troubleshoot process instrumentation including sensors, transmitters, valves, and analytical equipment to ensure reliable operation.Lead and support commissioning, qualification

and validation activities for control systems and instrumentation.Collaborate with manufacturing, quality, engineering, IT teams, and external suppliers to deliver effective technical solutions.Drive continuous improvement initiatives, conduct root cause investigations, and provide technical support and training to operational teams.What we are looking for:A degree in Electrical Engineering, Automation, Chemical Engineering, or a related technical discipline, or equivalent relevant experience.Significant experience in controls and instrumentation engineering, ideally gained within a biopharmaceutical, pharmaceutical, or other regulated manufacturing environment.Strong experience with PLC programming and troubleshooting, including platforms such as Rockwell Automation or Siemens.Experience working with Distributed Control Systems (DCS), particularly Emerson DeltaV, and HMI/SCADA platforms.Strong knowledge of process instrumentation principles, calibration techniques, troubleshooting
methodologies, and industrial communication protocols.Experience working in a GxP/cGMP regulated environment, with knowledge of computerized system validation (CSV) principles.Ability to interpret P&IDs, electrical schematics, and technical documentation, with excellent problem-solving and communication skills.About LonzaAt 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