Internship MSAT Upstream 80-100%

Lonza Group Ltd.

Oberwallis

Vor Ort

Vertraulich

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Agile career culture
Inclusive workplace
Performance-based compensation
Role/location benefits

Zusammenfassung

Lonza Group Ltd. in Visp, Switzerland, offers a 12‑month internship to support Process Experts in large‑scale biopharma manufacturing. This fully site‑based role emphasizes real‑time collaboration, data integrity, and GMP compliance to ensure high quality medicines.

You will assist technology transfer, data collection, documentation, and cross‑functional coordination with Manufacturing, MSAT, QA, and Process Development teams to drive process improvements.

Qualifikationen

  • Ongoing or completed Bachelor's or Master’s in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or related field.
  • Strong curiosity about biopharma manufacturing and process science (USP or DSP).
  • Basic understanding of bioprocessing and GMP is an advantage.

Aufgaben

  • Assist in technology transfer activities by helping prepare process documentation, tracking data, and coordinating cross‑functional input.
  • Support data collection and analysis for manufacturing batches, deviations, and process performance trends.
  • Help prepare presentations, reports, and process descriptions for internal stakeholders and customer interactions.
  • Participate in process risk assessments, change controls, and process improvement initiatives.
  • Collaborate with Manufacturing, MSAT, QA, and Process Development teams on daily operations and troubleshooting activities.
  • Maintain GMP documentation practices and ensure data integrity in support of regulatory compliance.
  • Attend and contribute to team meetings, taking notes, and following up on action items.

Kenntnisse

Biotech curiosity
English communication
Team player

Ausbildung

Bachelor’s or Master’s degree in Biotechnology or Life Sciences

Jobbeschreibung

The actual location of this job is in Visp, Switzerland. As part of this growth, we’re offering an internship opportunity to support our Process Experts and Senior Process Experts in large-scale mammalian upstream and downstream manufacturing. 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?

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