Batch Record Reviewer

Batch Record Reviewer

This is a fully site-based role based in Visp, Switzerland. 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:

• Ensure compliance and technical integrity across bioprocess manufacturing by conducting thorough reviews of executed electronic batch records in MES Syncade.

• Work closely with cross-functional Operations, Quality, and Automation teams to resolve discrepancies and clarify ambiguities in executed batch records.

• Drive continuous improvement by participating in MES Syncade recipe change management to optimize digital manufacturing workflows.

• Manage and support Quality Records, including CAPAs, Deviations, and Root Cause Investigations stemming from batch record review observations.

• Facilitate seamless product release by assembling, reviewing, and verifying the completeness of final documentation packages.

• Serve as a technical subject matter expert during direct customer interactions on batch record review and automation-related topics.

• Track operational excellence by regularly collecting, evaluating, and presenting key performance indicator (KPI) data.

What we are looking for:

• Educational background with a University degree in Biology, Biotechnology, Life Sciences, or a related field.

• Proven hands-on experience in electronic Batch Record Review within a Manufacturing Execution System (MES), specifically MES Syncade.

• Solid foundational understanding of Good Manufacturing Practice (GMP) principles and bioprocess manufacturing operational workflows.

• Demonstrated ability to identify non-compliance, technical gaps, and quality risks against established quality standards.

• Strong problem-solving mindset with experience investigating and managing Quality Records (Deviations, CAPAs).

• Professional fluency in English (written and spoken) with a highly structured, precise, and well-organized working style.

• Pragmatic, open-minded approach to continuous learning, process improvements, and cross-team collaboration.

About Lonza 

At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, 

Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. 

At Lonza, they 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. 

Ready to play your part in shaping the future of life sciences? Apply now.