Panel Discussion
Monday, September 23
06:30 PM - 07:15 PM
Live in Berlin
Less Details
New classes of biological medicines, new modalities and new industry pressures such as C&G therapy, small-scale, low-cost manufacturing plants, and continuous processing require a straight shift in biomanufacturing processes. If Pharma MES is located at the core of the Factory of the Future the industry needs to digitize and automate processes further and rely on the use of new technologies. Whereas i.e., C&G therapy is pushing digitalization and leads to new production IT strategies, current MES solutions are not as flexible, agile, and open as they need to be. So far, the pharmaceutical industry has not agreed on a common position but within the industry the movement from monolithic solutions to MES platform is visible.In this session, we will address the following questions:
Jeremy Tanner is Senior Director, Global Head of Quality Sales at Lonza. He is passionate about paperless execution in the cGMP manufacturing and QC spaces. Expansive QC microbiology and manufacturing experience have enabled development and enhancement of key software solutions in the cGMP arena. Jeremy is an experienced key account representative helping customers meet the challenging needs of recording information in a cGMP facility. He has enabled many customers to go paperless and enhance their compliance & data integrity.
David “Joey” Lutskus is a subject matter expert on MES solutions with over 20 years’ experience in the bio-pharmaceutical industry. Currently, IT Head of Cell and Gene COE at Lonza, Joey is responsible for leading all strategic initiatives, along with managing the project teams for the deployment of MODA-ES. The software has been deployed across four (4) Cell and Gene sites and two (2) Drug Product sites within Lonza. Previously, Joey worked in various roles across manufacturing modalities, supporting FormWeigh, SAP and Rockwell’s PharamSuite software. Joey is a member of the BioPhorum IT MES of the Future working team.