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.

Supports audit management and quality assurance activities at a cGxP contract manufacturing facility. Responsibilities include developing internal GxP auditing skills, supporting regulatory inspections and customer audits, preparing audit walkdowns, leading audit and inspection responses, managing complex deviation investigations, owning quality-process documents, becoming a qualified trainer, and serving as a subject matter expert. The role requires practical QA operations experience in a GMP-regulated biopharmaceutical environment and strong knowledge of quality systems and regulatory guidelines.

The Senior Specialist is responsible for leading technical reviews, ensuring compliance, mentoring junior staff, and supporting quality investigations related to assays and technologies in a life sciences environment.