Graduate Student

What you will do:

• 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.

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.