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 fully site-based role in Visp, Switzerland, is ideal for a motivated graduate or junior professional looking to make a direct impact in bioprocess manufacturing quality. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

• 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.