The Supply Chain Network Planner will integrate demand and supply plans, manage inventory optimization, and ensure effective collaboration with cross-functional teams to ensure product delivery.

The Senior Process Engineer will oversee technology transfer, process optimization, compliance, and documentation in the CGT division, ensuring GMP standards and collaborating with teams and clients.

The Lead Engineer, ODE - Automation is responsible for introducing and maintaining automation control systems for GMP biologics manufacturing, system administration, troubleshooting, process support, and ensuring regulatory compliance.

The trainee will work in Development Services focusing on cell culture, purification processes, and analytical testing, adhering to cGMP standards.

As a Biotechnologist, you'll handle GMP manufacturing, operate bioreactors, execute chromatography, and maintain lab standards while working on therapeutic protein production.

As a Biotechnologist, you'll perform GMP manufacturing operations and maintain facility standards while applying aseptic techniques and operating bioreactors.

As a CCP Trainee in the MSAT USP team, you'll assist with pre-campaign preparations, process monitoring, post-campaign reviews, and support commercialization efforts while collaborating with cross-functional teams.

Responsibilities include manufacturing therapeutic cell products under cGMP conditions, maintaining compliant production facilities, and conducting aseptic process simulations. Training will be provided, and the role involves physical activities in a cleanroom environment.

The Biotechnologist Trainee will assist in the manufacturing of therapeutic proteins under cGMP conditions, performing basic lab tasks, equipment monitoring, troubleshooting, and maintaining facility standards.

As an MSAT Intern, you will support upstream manufacturing processes, prepare for campaigns, monitor operations, and assist with performance reviews. You will gain hands-on experience in biotechnology under cGMP conditions.

The P2P Content Enablement Specialist supports content management processes and collaborates with procurement and supply chain teams, ensuring compliance and improving systems like Ariba and SAP ERP.

The trainee will conduct analytical testing for cell culture and purification teams, document results per GMP regulations, and perform general lab support duties.

As a Program Manager, you will lead complex programs between Lonza and customers, ensuring timely and quality delivery while fostering strong relationships.

As a trainee in Quality Control, you'll perform testing and analysis of products, maintain documentation according to cGMP, and support lab operations.

The CCP Trainee will support cell culture, purification, and analytical services in a biopharmaceutical environment, assisting with daily lab activities and adhering to cGMP regulations.

Provide daily Quality Assurance activities in a GMP Biotech Manufacturing facility, ensuring compliance, supporting investigations, and maintaining product quality.

The Senior Specialist in QA Compliance ensures quality in the supply chain by managing supplier qualifications, audits, and compliance with regulatory requirements. They lead investigations and operational improvements, collaborating with various stakeholders across departments.

The Biotechnologist will execute Cell Therapy production under cGMP conditions, performing tasks like culture preparation, harvesting, filling vials, and maintaining cleanroom standards.

The QA Specialist supports daily quality assurance tasks, reviews documentation, leads small projects, ensures compliance with GMP, and participates in audits and investigations.

Lonza seeks fresh graduates in Life Sciences or related fields for various roles, emphasizing problem-solving, communication, and teamwork skills.