Mammalian Upstream MSAT Internship

Lonza Group Ltd.; Oberwallis; Vor Ort; Vertraulich; Vollzeit

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

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.