Teams at Lonza

Ensure API production complies with GMP in a biopharmaceutical manufacturing environment. Responsibilities include reviewing manufacturing documentation, managing change controls, investigating deviations and OOS results, supporting quality management improvements, advising development and production teams, and serving as the quality contact during client GMP audits. The role also involves stakeholder management, contract manufacturing support, regulatory awareness, and project management.

Supervise QC microbiology personnel and daily testing operations in a cGMP manufacturing environment. Responsibilities include hiring, training, performance management, scheduling, testing oversight, documentation approval, regulatory compliance, OOS and CAPA investigations, continuous improvement, and audit support. The supervisor serves as both a people leader and technical subject matter expert while ensuring quality, safety, productivity, and operational objectives are met.

Supports 24/7 downstream biopharmaceutical manufacturing as a systems and equipment subject matter expert. Investigates technical issues, performs root cause analysis, leads improvement projects, supports equipment startup and qualification, analyzes process data, and contributes to CAPEX projects and new product transfers in a GMP-regulated environment.