Data Reviewer, Quality Control - HPLC Biologics

Review analytical data from HPLC and capillary electrophoresis (CE) analyses Evaluate quality parameters supporting stability studies and batch release Investigate unexpected or ambiguous results in collaboration with the QC laboratory team Ensure analytical data and associated documentation comply with GMP requirements, SOPs and internal procedures Support timely batch release through accurate and thorough data review

Join our international team and contribute to the quality of innovative biologic medicines.

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 for all employees.

• A BSc or MSc in chemistry, biochemistry or a related field, or equivalent experience

• Experience in a GMP-regulated Quality Control environment is highly preferred

• Hands-on experience with HPLC and/or CE techniques, including icIEF, is highly preferred

• Strong attention to detail and a precise, structured approach to reviewing analytical data

• An inquisitive mindset and the ability to critically assess and investigate unexpected results

• Flexibility to adapt to changing priorities in a fast-paced environment

• Fluency in English; German language skills are advantageous