Provide daily Quality Assurance support for GMP Biotech Manufacturing, ensuring compliance with SOPs, managing documentations, and participating in quality investigations.

The QA Specialist will oversee compliance, documentation, and product quality in a cGMP environment, supporting timely product releases and managing quality events.

Join Lonza as a trainee in quality control, focusing on testing, analysis, documentation, and operational efficiency in a lab environment.

The QC Analyst conducts microbiological testing, analysis of samples, ensures compliance with cGMP, troubleshoots methods and equipment, and supports laboratory operations.

The Program Manager will lead complex programs involving collaboration across teams, ensuring timely delivery and high-quality standards while advocating for customer needs.

The Biotechnologist Intern supports CGT manufacturing in a GMP environment, learns procedures, performs basic lab tasks, and maintains facility standards.