Laboratory Associate Commercial Quality Control

Perform basic operational tasks in the lab (e.g mobile phase preparations, calibration of pH meter, balance check). Ensuring cleanliness and tidiness in the laboratory. This includes adherence to 6S principles and to cGMP standards for audit readiness. Perform analytical testing within DPS Commercial QC (cGMP) for batch release and stability studies of drug products under cGMP according to existing method SOPs. Document assay performance following Good Documentation Practices (GDocP) and flag relevant observations to the supervisor for further assessment. Following applicable EHS regulations.

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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Training as lab technician (e.g. EFZ, CTA) or BSc in Analytical Chemistry, Biochemistry or related field

• Willingness to learn and grow

• Experience working in a GMP-regulated QC laboratory is a plus

• Experience with HPLC, CE-SDS, icIEF, or ELISA is a plus

• Understanding of cGMP, GDocP, and Data Integrity principles

• Excellent written and verbal communication skills in English