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Opportunities · Internship

Internship MSAT Downstream 80-100% (m/f/d)

Lonza · Visp, Switzerland

Applies on Workday≈$10-$20/hr

Dates for this one

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Posted

Aug 31, 2026

What matters in this listing

What you'll own

  • Assisting in technology transfer activities by helping prepare process documentation, tracking data, and coordinating cross-functional input.
  • Supporting data collection and analysis for manufacturing batches, deviations, and process performance trends.
  • Helping to prepare presentations, reports, and process descriptions for internal stakeholders and customer interactions.
  • Participating in process risk assessments, change controls, and process improvement initiatives.

Requirements and eligibility

  • Ongoing or completed Bachelor’s or Master’s degree or equivalent experience in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or a related field.

Preferred, not required

  • Strong communication skills in English; German is a plus.
Read the full listing context

The actual location of this job is in Visp, Switzerland. As an intern supporting the Process Expert team in Downstream area, you will gain hands-on exposure to biopharmaceutical manufacturing and technology transfer processes.

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.

Duration: 12 months. What you will get: • An agile career and dynamic working culture. • An inclusive and ethical workplace. • Compensation programs that recognize high performance.

• A variety of benefits dependent on role and location. What you'll do: • Assisting in technology transfer activities by helping prepare process documentation, tracking data, and coordinating cross-functional input.

• Supporting data collection and analysis for manufacturing batches, deviations, and process performance trends. • Helping to prepare presentations, reports, and process descriptions for internal stakeholders and customer interactions.

• Participating in process risk assessments, change controls, and process improvement initiatives. • Collaborating with Manufacturing, MSAT, QA, and Process Development teams on daily operations and troubleshooting activities.

• Maintaining GMP documentation practices and ensuring data integrity in support of regulatory compliance. • Attending and contributing to team meetings, taking notes, and following up on action items.

What we are looking for: • Ongoing or completed Bachelor’s or Master’s degree or equivalent experience in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or a related field.

• Strong curiosity about biopharma manufacturing and process science (USP or DSP). • Basic understanding of bioprocessing and GMP is an advantage. • Strong communication skills in English; German is a plus.

• Organized, detail-oriented, and a good teammate. • Comfortable working in a dynamic and fast-paced environment. 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.

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