The Reliability Engineer will improve equipment reliability, analyze maintenance data, and develop maintenance strategies to prevent downtime and enhance performance.

Lead Scientist overseeing purification process development and viral clearance, managing projects, and ensuring compliance with regulatory requirements.

The Biotechnologist role involves manufacturing therapeutic cell products under CGMP, maintaining clean room standards, and performing cell culture activities.

The Technical Specialist leads readiness and release operations in manufacturing, drives continuous improvements, and manages deviation investigations and compliance audits.

As a Biotechnologist, perform GMP manufacturing, operate bioreactors, apply aseptic techniques, and utilize process control systems to produce therapeutic proteins.

The Biotechnologist will perform manufacturing activities for CGT, ensure compliance with quality standards, and maintain GMP operations.

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

Lead technology transfer of purification processes, resolve technical challenges, and drive continuous improvement projects within a cross-functional team.

The Biotechnologist Trainee assists in the manufacturing of therapeutic proteins, performs laboratory tasks, and gains expertise in GMP operations and equipment.

The Program Manager will lead internal project teams at Lonza, manage project lifecycles, and ensure effective communication and execution of contracted programs, focusing on quality, timelines, and customer satisfaction.

The CCP Trainee role involves supporting the development of cell culture and purification processes in a laboratory environment, while adhering to safety and documentation standards under supervision.

As a Biotechnologist, you will perform GMP manufacturing, operate bioreactors, apply aseptic techniques, and handle quality control in a dynamic environment.

Conduct various testing and analysis tasks in QC, ensure compliance with cGMP, support investigations, and manage laboratory operations.

The Lead Engineer of ODE - Automation manages automation control systems for GMP manufacturing, ensuring administration, troubleshooting, and regulatory compliance.

The position involves laboratory support tasks, equipment verification, media preparation, documentation, and adherence to safety and quality regulations.

The Associate Manager, QC oversees biochemistry method transfer, ensures compliance and training, manages laboratory operations, and leads personnel development.

Lead and support the transfer of manufacturing processes to Lonza's facility, analyze processes, conduct experiments, and manage documentation and training.

The CCP6 Trainee performs microbiology techniques, supports testing and analysis, documents results, and assists in investigations while adhering to cGMP regulations.