Today Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. What you’ll get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be also found on. What you’ll do: Perform timely and independent review of executed electronic batch records (eBRs) in MES Syncade. Ensures that operations batch records are accurately executed, complete, and ready for QA review. Collaborate with Manufacturing and Quality teams to clarify and resolve documentation issues. Initiate and support in the management of Quality Records (CAPAs and Deviations) for Batch Record review related observations. Support preparation of documentation package to enable fast release by QA. What we’re looking for: Previous experience in GDP and GMP regulated pharmaceutical / API industry. Experience in batch record review (preferred eBR) OR in manufacturing is required. Ability to identify non-compliance and gaps from quality standards Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation. Structured, focused and well-organized working attitude. Open-minded for new ideas and suggestions; solution-oriented. Agile, highly motivated and dynamic drive. Every day, Lonza’s products and services have a positive