Support day-to-day Quality Assurance activities, ensure compliance, analyze data, manage documentation, and collaborate with teams on quality-related tasks.

The Biotechnologist Trainee will manufacture therapeutic proteins under cGMP, perform laboratory tasks, and support operations while adhering to safety and quality standards.

The Trainee will assist in developing cell lines, purification processes, and analytical testing under supervision, adhering to Good Manufacturing Practices and regulations.

The Biotechnologist Intern supports therapeutic protein manufacturing under cGMP conditions, performing laboratory tasks and maintaining facility standards while gaining experience in a biotech environment.

The Biotechnologist is responsible for manufacturing cell therapy products in compliance with cGMP regulations, performing environmental monitoring and maintaining accurate documentation, while working in cleanroom environments and rotating shifts.

The Process Data Expert will utilize advanced data science techniques to develop analytical tools, solve bioprocessing problems, and improve data utilization at Lonza.

This role focuses on driving operational excellence and process improvements through Lean Six Sigma methodologies, coaching teams, and managing stakeholder projects. Responsibilities include leading continuous improvement initiatives and facilitating training based on best practices.

Perform GMP manufacturing operations and maintain laboratory standards. Operate bioreactors and execute chromatography operations, ensuring compliance with cGMP standards.

The Group Lead of Program Management will oversee multiple projects, manage teams, ensure timely delivery, and liaise with stakeholders to align project goals with business objectives.

The Senior Process Engineer will lead the transfer of cell culture processes, support operations, investigate trends, and ensure compliance with standards.

The QA Specialist will support Quality Assurance activities in a GMP biotech manufacturing facility, ensuring compliance, leading investigations, and coordinating with departments.

The CCP Trainee will assist in the development of purification processes and contribute to laboratory activities related to biotechnology, with a focus on cell culture and protein sample preparation.

As a Process Development Engineer, you will lead technology transfer and process support in manufacturing, ensure process robustness, and perform investigations into deviations.

Lead multidisciplinary project teams to ensure smooth execution of contracted programs, focusing on customer satisfaction, quality, cost, and timelines.

The Biotechnologist Trainee is responsible for manufacturing therapeutic proteins under GMP conditions, performing laboratory tasks, troubleshooting, and maintaining equipment compliance.

Oversee harmonization projects across global network sites, provide technical support and coaching, and maintain compliance knowledge to improve operational execution.

The MSAT Intern will support the monitoring and analysis of cell culture and purification processes, assist in data collection, and participate in process investigations while learning about cGMP environments.

The QC Analyst will perform various testing and analysis, ensure cGMP compliance, solve analytical problems, and support laboratory operations.

The Biotechnologist will perform GMP manufacturing operations, handling equipment and troubleshooting, operating bioreactors, and preparing solutions for production while adhering to cGMP standards.

The QC Analyst will perform microbiological tests, analyze samples, document results per cGMP guidelines, and assist with method transfers and validations.