Batch Record Reviewer

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Batch Record Reviewer

Batch Record Reviewer Are you looking to make a direct impact on the delivery of life-saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. 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:

What you will do:

What we are looking for:

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.

Münchensteinerstrasse 38 4052 Basel

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• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Ensure the timely release and compliance of life-saving medicines by performing rigorous batch record reviews.
• Partner with cross-functional teams, including Manufacturing and Quality, to investigate and resolve batch discrepancies.
• Analyze electronic and paper-based batch records within state-of-the-art MES (Syncade), DeltaV, SAP, TrackWise, and LIMS environments.
• Evaluate process parameter failures, material consumption, and operator comments in strict alignment with ALCOA+ and GDP principles.
• Draft clear, compliant quality impact statements and author post-production lifecycle documentation.
• Drive continuous improvement and data integrity standards across site production lines.
• Degree in Life Sciences, Biotechnology, or a related scientific discipline (or equivalent practical experience).
• Proven track record working within a GMP-regulated manufacturing or quality assurance environment.
• Hands-on experience with electronic batch record systems (MES Syncade, DeltaV) and quality management systems (TrackWise, SAP, LIMS).
• Solid understanding of Documentation Practices (GDP) and ALCOA+ data integrity principles.
• Strong problem-solving mindset with the ability to work independently and meet strict production deadlines.
• Fluency in English (written and spoken) is required; reading proficiency is a strong advantage.
• Lonza Group AG