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

You drive the successful transfer and implementation of aseptic fill‑&‑finish processes at our manufacturing site and lead projects that expand and enhance our capabilities across the network. You own complex concepts end‑to‑end and continuously strengthen quality and efficiency — always in full compliance with GMP. Join us to make a real impact on how we manufacture life‑changing medicines. Check out Your Career in Drug Product Services at Lonza!

What you will get:

• An agile career and a dynamic work culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

• Benefits in Stein: https://bit.ly/42DlBDk

What you will do:

• Lead technical transfers for aseptic fill&finish processes by evaluating and developing fit‑for‑purpose processes and applying structured tools to manage information transfer, process‑related risks and change control.

• Act as process owner , proactively identifying and resolving technical challenges, driving process monitoring and control strategies, and performing complex data analyses.

• Lead cross‑functional projects to enhance or expand manufacturing capabilities at the site and within the DPS network, including equipment, filling line and facility qualification as well as PPQ support for BLA projects.

• Manage complex deviations and complaints , using scientific and statistical insights to analyze data, understand processes and identify root causes of failures.

• Ensure inspection readiness , supporting internal and external audits, contributing to front/back‑office activities and representing the area during facility tours.

• Coach and mentor MSAT colleagues , supporting them in project leadership and in driving concept implementation across the site and network.

What we are looking for:

• Solid experience in aseptic/sterile manufacturing processes of drug products in a GMP environment is a must, with substantial know-how in aseptic processing and sterility assurance principles.

• Experience in qualification of manufacturing equipment, cleaning validation, and room qualification is an asset.

• University Degree or equivalent technical education in Biotechnology, Pharmacy, or equivalent experience.

• Strong communication skills, able to translate complex technical topics into clear actionable messages.

• Proactive, positive approach, problem-solving attitude, and ability to take full responsibility for assigned areas.

• Ability to lead cross-functional teams and drive decision-making in a matrix organization; build strong networks and trust across internal and external stakeholders.

• Proficiency in English is a must; German language skills are a plus.

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.

Ready to shape the future of life sciences? Apply now.