Batch Record Reviewer

Are you looking to make a direct impact on the production of life-changing therapies? Join our dynamic team in Visp as a Batch Record Reviewer, where you will ensure the execution accuracy and compliance of electronic batch records in MES Syncade to support timely product releases.

1 to 2 years of experience in MES/DeltaV batch record support or administration (graduates with relevant experience are also welcome).

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, independent reviews of executed electronic batch records (eBRs) in MES Syncade to ensure high Quality Assurance readiness.

• Verify that all manufacturing process steps are performed as intended and fully compliant with Good Documentation Practice (GDP) standards.

• Identify, document, and support the resolution of execution gaps, non-compliances, and discrepancies on the shop floor.

• Support the management and timely closure of Quality Records, including CAPAs, Deviations, and Investigations.

• Collaborate directly with Operations to troubleshoot batch execution issues and participate in continuous MES Syncade recipe improvements.

• Drive timely batch releases by ensuring complete, error-free documentation and prompt issue resolution.

• Contribute to cross-functional alignment between Manufacturing and Quality to foster operational excellence.

What we are looking for:

• Bachelor’s degree or equivalent qualification in Pharmacy, Engineering, Biotechnology, or a related technical field.

• 1 to 2 years of experience in MES (DeltaV) batch record support or administration (graduates with relevant MES/DeltaV experience are also welcome).

• GMP background required, with experience from any regulated manufacturing environment (pharma background is not strictly required).

• Strong analytical ability to identify compliance non-conformances, quality gaps, and documentation errors.

• Professional fluency in English; basic German proficiency (A2) or a strong willingness to learn on the job.

• Structured, precise, and well-organized approach to work with a high commitment to detail.

• Open-minded, pragmatic, and proactive attitude toward adopting new tools and recipe improvements.

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.

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