Conduct hands-on lab work in protein purification and process development, ensuring quality standards under cGMP regulations, leading projects, and drafting documentation.

The Operational Buyer manages Raw Material specifications, oversees supplier performance, leads Change Requests, and ensures compliance with regulatory standards.

The Associate Manager, QC leads testing supervision, data review, and communication with agencies while ensuring cGMP compliance and vendor evaluations. This role involves training staff and conducting performance evaluations.

The QA Expert oversees daily Quality Assurance activities in a cGMP manufacturing facility, ensuring compliance with SOPs and coordinating departmental efforts.

The Technical Specialist leads manufacturing operations, manages readiness for processes, supports audits, investigates deviations, and drives continuous improvement.

The role involves executing analytical testing, interpreting data, and ensuring compliance with ICH and GMP guidelines in protein characterization.

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 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.

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

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.