Biopharma Batch Records Intern – QA & GDP

Lonza Group AG; Eyholz; Vor Ort; CHF 50.000 - 65.000; Vollzeit

Benefits dieser Stelle

An agile career and dynamic working文化.

An inclusive and ethical workplace.

Zusammenfassung

Lonza Group AG in Visp, Switzerland, seeks a Graduate Student – Intern – Batch Record Reviewer to support timely eBR reviews within MES Syncade for Module P Bufferprep, contributing to GDP‑compliant batch closures and QA readiness.

This site‑based role offers hands‑on bioprocess manufacturing experience, cross‑functional collaboration, and exposure to state‑of‑the‑art facilities, with emphasis on quality, documentation, and patient safety.

Qualifikationen

• Bachelor’s degree or equivalent in a life sciences field.
• Foundational understanding of GMP principles.
• Experience with batch record review (eBR) or biomanufacturing.
• Familiarity with MES systems, preferably MES Syncade.
• Strong analytical mindset and attention to documentation.

Aufgaben

• Perform timely and independent reviews of executed electronic batch records (eBRs) within MES Syncade for Module P Bufferprep.
• Safeguard patient safety and quality by ensuring all operations batch records are accurately executed, complete, and prepared for QA release.
• Verify that bioprocess manufacturing steps were conducted as intended and align with GDP standards.
• Identify, investigate, and resolve non‑compliance issues before final batch release.
• Collaborate with cross‑functional manufacturing and QA teams on site to enable rapid batch closure cycles.
• Gain exposure to a state‑of‑the‑art biopharmaceutical manufacturing environment.

Kenntnisse

GMP principles

Batch record review

MES Syncade

Analytical thinking

English fluency

German basics

Ausbildung

Bachelor's degree or equivalent in Life Sciences

Tools

MES Syncade

Jobbeschreibung

Lonza Group AG in Visp, Switzerland, seeks a Graduate Student – Intern – Batch Record Reviewer to support timely eBR reviews within MES Syncade for Module P Bufferprep, contributing to GDP‑compliant batch closures and QA readiness.

This site‑based role offers hands‑on bioprocess manufacturing experience, cross‑functional collaboration, and exposure to state‑of‑the‑art facilities, with emphasis on quality, documentation, and patient safety.