After an onboarding period in Visp, Switzerland, the position will be based in the U. S . (East or Mi d -W est Coast) to support the expansion of small molecules/bioconjugation capabilities. Relocation targeted in Q1 2027 and assistance is available for eligible candidates and their families, if needed.

In this role, you will have a direct impact by optimizing daily GMP operations, improving process robustness, and ensuring safe, compliant, and timely production. You will also play a key role in capability expansion—supporting equipment introductions, authoring critical documentation, and resolving issues through data driven problem solving and cross functional collaboration.

What you will get :

• An agile career and dynamic working culture, with the opportunity to work on an international assignment

• A highly collaborative environment that fosters teamwork and inclusion

• A range of professional development programs to grow your skills and career

• An ethical workplace where tasks are carried out in accordance with relevant procedures

• The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits .

What you will do:

• Lead the day-to-day execution of manufacturing activities in a GMP environment, helping ensure safe, reliable, and high-quality operations.

• Partner closely with cross-functional teams to support the introduction of new equipment and capabilities, including user requirements input and participation in key project milestones such as FAT and SAT.

• Prepare manufacturing areas for successful operations by updating documentation, ensuring equipment readiness, and performing standard checks before batch activities.

• Provide guidance and on-the-job training to colleagues on new processes, safety practices, and good documentation behaviors , helping foster a culture of learning and team development.

• Support troubleshooting and problem-solving with engineering, quality, and technical experts to keep operations running smoothly and implement effective improvements.

• Use practical continuous-improvement tools to simplify processes, enhance efficiency, and strengthen overall performance of equipment and workflows.

• Represent the manufacturing area confidently during audits, technical transfers, and early production campaigns linked to newly introduced technologies.

What we are looking for:

• Bachelor’s degree in a scientific or engineering field—or equivalent relevant experience and learning gained through industry roles.

• Experience working in GMP manufacturing, pharmaceutical operations, biotechnology, or a similar regulated environment.

• Ability to contribute to equipment and process introduction activities, with familiarity in areas such as FAT/SAT and qualification steps considered beneficial.

• Clear and supportive communication skills, with the ability to train and collaborate with colleagues across functions and levels.

• A practical approach to problem-solving, using structured methods to identify root causes and drive improvements.

• A proactive, organized mindset, with the ability to balance multiple activities while maintaining a commitment to safety, quality, and continuous improvement.

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 are 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 .