Batch Record Reviewer

Batch Record Reviewer

Batch Record Reviewer

Batch Record Reviewer

Are you ready to accelerate the delivery of life‑saving therapies by ensuring seamless batch record closures in our buffer preparation facility? This is a fully site‑based role in Visp, Switzerland, ideal for a motivated graduate or junior professional looking to make a direct impact in bioprocess manufacturing quality.

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.

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 e ) 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.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

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