Teams at Lonza

Lead QA Audit Specialist to support audit activities and GMP/cGxP compliance at a multi-product contract manufacturing site. Responsibilities include internal GxP auditing, inspection and customer audit support, audit walkdown preparation, audit/inspection responses, leading complex deviation investigations, owning assigned quality process documents, and serving as subject-matter expert and trainer.

The QA Specialist ensures compliance with GMP standards in manufacturing, reviews quality documents, leads investigations, and manages relationships with teams and partners.

The trainee will receive structured on-the-job training in technology transfer, document management, and collaboration with project engineers in the biopharmaceutical industry.