Batch Record Reviewer

ph3bBatch Record Reviewer /b /h3 pBatch Record Reviewer /p pBatch Record Reviewer /p pAre 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. /p pThis 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. /p pWhat you will get: /p pAn agile career and dynamic working culture. /p pAn inclusive and ethical workplace. /p pWhat you will do: /p pPerform timely and independent reviews of executed electronic batch records (eBRs) within MES Syncade for Module P Bufferprep. /p pSafeguard patient safety and quality by ensuring all operations batch records are accurately executed, complete, and fully prepared for QA release. /p pVerify that bioprocess manufacturing steps were conducted as intended and align strictly with Good Documentation Practice (GDP) standards. /p pProactively identify, investigate, and resolve non‑compliance issues, gaps, or discrepancies prior to final batch release. /p pCollaborate closely with cross‑functional manufacturing and Quality Assurance teams on site to ensure rapid batch closure cycles. /p pGain high‑visibility experience and develop professional expertise within a state‑of‑the‑art biopharmaceutical manufacturing environment. /p pWhat we are looking for: /p pEducational background with a Bachelor’s degree or equivalent in Pharmacy, Engineering, Chemistry, or a related technical life sciences field. /p pFoundational understanding of Good Manufacturing Practice (GMP) principles and bioprocess manufacturing processes. /p pPractical experience in batch record review (preferably eBR) or direct hands‑on biomanufacturing experience. /p pFamiliarity with Manufacturing Execution Systems (MES), ideally MES Syncade. /p pStrong analytical mindset with the ability to spot documentation gaps, non‑compliance, and quality discrepancies. /p pFluency in English (spoken and written); basic German proficiency (A2) is beneficial. /p pA structured, precise, and well‑organized approach to work combined with a pragmatic, problem‑solving attitude. /p pAbout Lonza /p pAt 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. /p pInnovation 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. /p pAs Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role. /p ul libWork location /b 3930 Eyholz (VS) /li libWorkload /b 100% /li libEmployment start /b By agreement /li libEmployment duration /b Temporary /li libBy online /b Online form /li /ul /p #J-18808-Ljbffr