Graduate Student

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

Graduate Student

The Graduate Student – Intern – Batch Record Reviewer role focuses on ensuring seamless batch record closures in our buffer preparation facility. This fully site‑based position in Visp, Switzerland is ideal for a motivated graduate or junior professional looking to make a direct impact in bioprocess manufacturing quality. Working in person supports close, real‑time collaboration and the technical precision needed to produce medicines to the highest quality and safety standards.

What you will get:

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.

What you will do:

• 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 fully prepared for QA release.
• Verify that bioprocess manufacturing steps were conducted as intended and align strictly with Good Documentation Practice (GDP) standards.
• Proactively identify, investigate, and resolve non‑compliance issues, gaps, or discrepancies prior to final batch release.
• Collaborate closely with cross‑functional manufacturing and Quality Assurance teams on site to ensure rapid batch closure cycles.
• Gain high‑visibility experience and develop professional expertise within a state‑of‑the‑art biopharmaceutical manufacturing environment.

What we are looking for:

• Educational background with a Bachelor’s degree or equivalent in Pharmacy, Engineering, Chemistry, or a related technical life sciences field.
• Foundational understanding of Good Manufacturing Practice (GMP) principles and bioprocess manufacturing processes.
• Practical experience in batch record review (preferably eBR) or direct hands‑on biomanufacturing experience.
• Familiarity with Manufacturing Execution Systems (MES), ideally MES Syncade.
• Strong analytical mindset with the ability to spot documentation gaps, non‑compliance, and quality discrepancies.
• Fluency in English (spoken and written); basic German proficiency (A2) is beneficial.
• A structured, precise, and well‑organized approach to work combined with a pragmatic, problem‑solving attitude.

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.

• Work location 3930 Eyholz (VS)
• Workload 100%
• Employment start By agreement
• Employment duration Temporary

• By online Online form