Location. Visp, Switzerland.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Based at our manufacturing site, this MSAT role offers the opportunity to take ownership of complex aseptic manufacturing processes from technology transfer to routine production. You will work closely with global teams and customers to ensure reliable, compliant, and high-quality drug product supply

What you will do:

• Responsible for implementing the manufacturing process in the plant, as received from DP process development or the customer.

• Lead and/or participate in cross-functional teams as an MSAT expert. This includes the lifecycle of assigned projects, from planning through coordination, implementation, control, and completion, aligned with project management goals.

• Act as technical counterpart to commercial and clinical customer.

• Owner of concepts for process controls and important areas within manufacturing.

• Act as singe-point-of-contact for operational topics within the Lonza network.

• Prepare and perform qualification and validation activities in compliance with cGMP regulations and specification requirements.

• Contribute to the development and implementation of standardized MSAT procedures and processes.

• Responsible for continuous improvement of process performance and product quality.

• Proactively anticipate, evaluate, and resolve scientific and technical challenges

• Act as a mentor for scientific and production staff across various fields of expertise.

• Manage process monitoring and process control strategies, including complex data analysis.

What we are looking for:

• Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering, or a related scientific discipline.

• More than 3 years of experience in manufacturing and/or MSAT, Development or QA/QC.

• Fluency in English (spoken and written).

• Proven understanding of aseptic manufacturing processes (pharmaceutical and regulatory aspects) is an advantage.

• Strong communication skills and ability to interact with various internal and external stakeholders.

• Clear team orientation and ability to collaborate across functional groups.

• Structured, focused, and well-organized working style.

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.