QC Analyst Intern 80-100% (m/f/d)

Today, Lonza is a global leader in life sciences operating across five 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.

At the Visp site, we are looking for an intern to join the day‑shift team of the 24/7 Analytical Services Laboratory (QC Biologics) for a duration of 6–12 months. In this role, you will take responsibility for document verification processes as well as the distribution of all laboratory samples. You will gain a holistic overview of the wide range of activities within the 24/7 Analytical environment and will have the opportunity to contribute to dedicated study work. In addition, you will obtain valuable insights into the daily challenges and responsibilities of a GMP-regulated laboratory at our steadily expanding Visp campus. For candidates who demonstrate strong performance—and depending on operational needs—there may be an opportunity to transition into a long‑term position within the 24/7 Analytical Services day team.

What you will do:

• Verification of printed analytical protocols
• Review of samples with status “H” in LIMS (for designated projects)
• Verification of reserve samples, shipment samples, and retention samples
• Issuing reserve and stability samples
• Creation and verification of label data
• Data extraction from LIMS / MODA systems
• Support in laboratory organization, including material coordination, sample logistics, and maintaining documentation structures
• Execution and monitoring of documentation activities in line with GMP requirements (e.g., filing, archiving, document tracking)
• Structured data transfer and documentation workflows using digital platforms such as SharePoint
• Contributing to continuous improvement by helping streamline processes, documentation flows, and sample management procedures

What we are looking for:

• Completed Bachelor’s degree (BSc)  or Master's degree (Msc) in a scientific discipline or equivalent qualification
• Initial experience in the pharmaceutical industry is an advantage
• Understanding of GMP principles, ideally with some practical exposure
• A motivated, proactive individual who is eager to take on new challenges
• A reliable team player with strong attention to detail and a hands‑on mindset
• Someone who enjoys learning, takes ownership of their tasks, and contributes positively to a dynamic laboratory environment
• Strong command of both German and English

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.