Perform testing and analysis to support business requirements, document results per cGMP, troubleshoot methods, and provide lab support.

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

The Biotechnologist oversees manufacturing therapeutic proteins under cGMP conditions, performing procedures, equipment monitoring, basic lab tasks, and troubleshooting while ensuring compliance with standards in a clean room environment.

The role involves supporting laboratory operations, ensuring compliance with GMP, equipment maintenance, and preparation of solvents and reagents.

Assist the Operational Buyer with daily tasks including order status review, data entry, presenting insights, and optimizing supply chain processes. Gain hands-on experience with SAP and various data management tools.

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

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

Oversee testing techniques, review lab data, author change controls, perform equipment validation, and coach junior staff. Engage with regulatory bodies and participate in audits.

As a Senior Principal Scientist, lead projects in bioprocess development at Lonza, mentoring teams and driving technology change across global networks.

The Engineer 2, Control Systems will maintain and support computerized systems for GMP manufacturing, ensuring system integrity, compliance with regulations, troubleshooting issues, and collaborating with teams for successful operations.

The QA Manager ensures QA oversight of Aseptic Processing and microbial control in cell and gene therapy, ensuring regulatory compliance and expertise in sterility assurance.

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.

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 an Expert in Operational Excellence, you will lead OE strategies, drive continuous improvement projects, and mentor teams using Lean Six Sigma methodologies to enhance performance.

Manage asset Program Management function, develop high-performing teams, ensure program delivery, maintain customer relationships, and drive financial accountability.