Join our webinar to learn more about
- Lonza’s development environment, design control, and innovation processes
- Challenges of risk management, change control, traceability in BioTech development
- Modernizing the development toolchain
- Building a single source of truth for product development
Associate Director, RnD Engineering, Bioscience, Lonza Cologne GmbH
Managing the intertwined development processes of hardware and software components in the design of medical technology is a challenge. For most teams, it is a challenge to navigate the complexity of MedTech product development with the necessary design controls in place throughout the lifecycle. Using a mix-and-match toolchain, ensuring traceability, managing approvals, catching risks, and tracking the impact of changes are all difficult to achieve.
To tackle those challenges and to reduce development times and effort costs, Lonza (a Swiss multinational pharma & biotech company) replaced its legacy system of MS Excel, Word, and other tools with modern, integrated digital tooling. Join this webinar with Lonza’s expert Timo Gleissner to find out how the company is mastering Product Lifecycle Management complexity by integrating hardware and software development in a collaborative, digital environment.
About the speaker
Timo Gleissner joined Lonza in April 2008 as a development engineer and as Associate Director (RnD Engineering, Lonza Bioscience). Him and his group are responsible for the technical development of the Nucleofector Products. Timo led several development projects for the Lonza Nucleofector family and holds a diploma in Electronics Engineering from RFH University of Applied Sciences Cologne, Germany.