Automation Engineer MES/DeltaV

Job-Room; Lalden; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Benefits dieser Stelle

Career growth

Collaborative workplace

Competitive compensation

Global benefits

Cutting-edge tech

Zusammenfassung

Lonza is seeking an Automation Engineer MES/DeltaV for its Visp, Switzerland site. You will implement, optimize, and support MES and DeltaV processes within biopharmaceutical manufacturing, ensuring production efficiency, regulatory compliance, and high-quality outcomes.

The role is fully site-based, requiring close collaboration across Manufacturing, Process Development, Automation, and Quality teams. You will develop validation records, provide end-user training, and drive continuous

Qualifikationen

• Experience in regulated pharma manufacturing environments.
• Knowledge of MES platforms including Werum PAS-X or PharmaSuite.
• Experience with DeltaV or other distributed control systems.
• Understanding of GMP, computerised system validation and qualification activities.

Aufgaben

• Design, implement, and validate MES recipes and DeltaV control strategies for compliant biopharma manufacturing.
• Collaborate with Manufacturing, Process Development, Automation, Engineering, and Quality teams for seamless integration.
• Troubleshoot MES and DeltaV issues to minimize production disruptions.
• Develop and maintain technical documentation in line with GMP requirements.
• Train end users and provide ongoing system expertise.
• Drive continuous improvement in manufacturing processes and automation performance.
• Support adoption of new digital manufacturing technologies.

Kenntnisse

DeltaV

MES

GMP understanding

Ausbildung

Bioprocess Engineering

Electrical Engineering

Tools

Werum PAS-X

Rockwell PharmaSuite

DeltaV

Jobbeschreibung

Automation Engineer MES/DeltaV

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

As a Automation Engineer MES / DeltaV, you will be responsible for the implementation, optimization, and ongoing support of Manufacturing Execution Systems (MES) and Emerson DeltaV process control systems within biopharmaceutical manufacturing facilities. You will play a key role in ensuring efficient production operations, regulatory compliance, and adherence to the highest quality standards.

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 with opportunities for professional growth in a global life sciences organization.
• A collaborative, inclusive, and ethical workplace where diverse perspectives are valued.
• Competitive compensation and recognition programs that reward high performance.
• Access to a wide range of local and global benefits, depending on role and location.
• Opportunities to work with cutting‑edge technologies in biopharmaceutical manufacturing and automation.
• The full list of our global benefits can be found here:

Responsibilities

• 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.

What we are looking for

• Experience working in the pharmaceutical, biopharmaceutical, biotechnology, or other highly regulated manufacturing environments.
• Strong knowledge of Manufacturing Execution Systems (MES), ideally including Werum PAS-X, Rockwell PharmaSuite, or comparable platforms.
• Experience with Emerson DeltaV or other distributed control systems used in process manufacturing.
• Understanding of GMP regulations, computerized system validation, and qualification activities in regulated industries.
• Ability to analyze complex technical issues, identify root causes, and implement effective solutions.
• Strong communication and collaboration skills, with the ability to work effectively across multidisciplinary teams.
• A degree in Bioprocess Engineering, Biotechnology, Automation Engineering, Electrical Engineering, or a related technical discipline, or equivalent experience demonstrating these capabilities.

About Lonza

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.

Lonza Group AG Münchensteinerstrasse 38 4052 Basel