Biomanufacturing World Summit

Edgardo Hernandez (he/him/his) is executive vice president at Eli Lilly and Company and president of manufacturing operations.

Ed served as senior vice president of global parenteral drug product, delivery devices and regional manufacturing from 2018 until 2021. In this role, he was responsible for global parenteral manufacturing, emerging markets manufacturing, drug-product contract manufacturing, packaging, and distribution operations. Ed provided oversight for manufacturing sites in 12 countries across North America, South America, Europe, and Asia; that manufacture the final parenteral product (non-oral) formulations of Lilly medicines.

Previously, Ed was vice president of Fegersheim Operations for Lilly’s manufacturing site located in France. Before that, he served as site head for two other Lilly manufacturing sites: Indianapolis Active Pharmaceutical Ingredient manufacturing from 2014 until 2016, and PR06 in Puerto Rico from 2012 until 2014. Ed joined Lilly in 2005 as an engineering services leader for Lilly del Caribe in Puerto Rico, after working for several years in positions for Pfizer and Pharmacia.

Ed is a native of Puerto Rico and holds bachelor’s and master’s degrees in chemical engineering from the University of Puerto Rico and North Carolina State University, respectively.

Brendan O’Callaghan leads Sanofi’s Manufacturing and Supply organization, a global network of close to 40 internal manufacturing sites, supported by a network of strategic external supply partners. Sanofi’s ambition is to build an Industry leading manufacturing and supply chain capability, based on a future-ready organization and network that will ensure the flawless launch of Sanofi’s rich and diverse late-stage pipeline and the continued, reliable supply of essential, high-quality, affordable and sustainable medicines and vaccines for patients, worldwide. Sanofi will leverage the latest in scientific, digital, technology and workforce solutions to achieve this ambition.

Brendan joined Sanofi in 2015 as Global Head of Biologics, later taking leadership of the integrated Manufacturing and Supply network supporting our Specialty Care portfolio, prior to taking on his current responsibilities in September 2021. He has played a key role in enabling Sanofi’s transformation to a fully integrated BioPharma company and advancing the modernization and digital transformation of our manufacturing teams and network, building capabilities and capacities to support Sanofi’s growth in Biologics, Vaccines and Small Molecule Manufacturing, as highlighted by continued investments into state of the art, digitally advanced and future ready facilities such as the 2020 ISPE Facility of the Year award winning site in Framingham, MA and Sanofi’s agile and industry leading Modulus platforms in Neuville (FR) and Singapore.

Prior to Sanofi, Brendan worked with Merck / MSD, Mallinckrodt and Schering-Plough, where he led Tech Ops organizations of increasing scope and responsibility, across a variety of site and global leadership roles.

Brendan graduated in Chemical Engineering from the University College of Dublin, where he currently serves as an honorary adjunct Professor of Chemical and Biochemical Engineering.

He is married with four sons. A keen sports enthusiast, Brendan is a UEFA qualified soccer coach.

Sanat Chattopadhyay is responsible for the company’s (approx.  $64 billion revenue) worldwide manufacturing and supply operations across a global network of sites for pharmaceuticals, vaccines, biologics and animal health products. Merck is known as MSD outside of the U.S. and Canada.

Sanat joined Merck in 2009 as Senior Vice President of Global Vaccines & Sterile Manufacturing Operations, spearheading the transformation of manufacturing and supply chain to grow and globalize its Vaccine business. Under Sanat’s leadership, Merck is currently executing a significant expansion of its biologics and vaccines manufacturing capacity with planned capital investments of more than $20 billion from 2020 through the end of 2024, to reach more patients around the globe.

Before joining Merck, he served as Senior Vice President, Technical Operations & Product Supply, for Wyeth Pharmaceuticals. Previously, he worked at Aventis and its predecessor companies as Senior Vice President, Industrial Operations, having served in many positions with increasing responsibilities for global supply chain, technology and manufacturing sites across North America, Europe and Asia Pacific. Sanat started his career with Hoechst Pharmaceuticals in 1983 and worked in many senior leadership assignments.

Sanat is a graduate in Chemical Engineering and holds a post-graduate degree in Industrial Engineering from India.

Outside of Merck, Sanat is a member of the Board of Directors of Ashland Inc.

Dr. Pat Yang is one of the most accomplished biotech manufacturing executives and technical operations leaders in the industry.

From 2017 to 2019, Pat was executive vice president at Juno Therapeutics, a leading CAR-T biotech company (now part of BMS) based in Seattle.

Previously, from 2009 to 2013, Pat was Executive Vice President and Global Head of Technical Operations at F. Hoffman-La Roche based in Basel, Switzerland. In this role, he was responsible for Roche’s biopharma process research and development, analytical sciences, engineering, quality, technical regulatory, supply chain and all manufacturing plants with approximately 15,000 employees around the world. From 2003 to 2009, Pat was Executive Vice President of Product Operations at Genentech. He assumed his role as Global Head of the combined technical operations of Roche and Genentech upon the acquisition of Genentech by Roche in 2009.

Before Genentech, Pat worked for 11 years at Merck & Company from 1992 to 2003, based in New Jersey, in various leadership positions including vice president of Asia Pacific Operations and vice president of Global Supply Chain Management. Prior to joining Merck in 1992, Pat spent 12 years at General Electric, serving in research, engineering, technology, and manufacturing leadership roles with increasing scope of responsibilities.

Pat holds a Bachelor of Science from the National Chiaotung University in Taiwan, a Master of Science from the University of Cincinnati, and a Ph.D. in engineering from Ohio State University.

Pat is a member of the Board of Directors of three public companies, Amyris, Codexis and PharmaEssentia. In addition, he is on the board of several private companies, including Acepodia, AltruBio, Antheia and Sana Biotechnology.

Susan Abu-Absi, Ph.D. is a strategic operations executive with over 20 years of experience in product development and supply in the biopharmaceutical industry. She joined Be Bio in March 2025 as Chief Operating Officer, responsible for driving all operational aspects of the business to unleash the power of engineered B cell medicines as therapeutics for patients with serious diseases.

Prior to Be Bio, Susan was Chief Technology Officer at 2seventy bio where she led the Technical Development, Supply & Quality organization. Her team provided deep execution capabilities in autologous cell therapy manufacturing resulting in the launch of Abecma and the translation of four novel therapies with complex layered technologies into the clinic.

Prior to 2seventy bio, Susan led technical development & operations at bluebird bio, a pioneer in ex vivo gene therapies, where she played an integral role in the approvals of Zynteglo and Skysona.

Prior to joining bluebird, Susan held leadership roles in the Global Product Development and Supply organization at Bristol Myers Squibb. She started her career in the Process Sciences organization at Bayer Healthcare.

Susan earned a Ph.D. in Chemical Engineering from the University of Minnesota, where she conducted research in the laboratory of Professor Wei-Shou Hu as a National Science Foundation Fellow, and a B.S. in Chemical Engineering, Summa Cum Laude with Honors, from the University of Toledo.

Dr. Advant has served as Savara’s Executive Vice President, Global Technical Operations since March 2024. With approximately three decades of experience in the biopharmaceutical sector, he has considerable expertise in drug substance, drug product, and analytical development with early- and late-stage clinical and commercially approved biologics. Dr. Advant also has extensive expertise in technology transfer, scale-up and cGMP manufacturing (both internal and external) in a highly regulated environment. To date, Dr. Advant has helped launch multiple biologic assets across several therapeutic areas. Prior to joining Savara, he was VP, Manufacturing Operations at GSK, where he was responsible for multi-site drug substance and drug product operations. Previously he held roles of increasing responsibility at Celgene Corporation (acquired by Bristol Myers Squibb), Kemwell BioPharma, ImClone/Lilly, and Diosynth Biotechnology (now FujiFilm Diosynth Biotechnolgy), among others. Dr. Advant holds a Ph.D. in Pharmaceutics from the University of Connecticut.

Andrea (Andi) Goddard serves as Chief Technical Officer at CatalYm. She brings three decades of global biotechnology experience, spanning all levels of operations — from the manufacturing floor to the C-suite. Andi joined CatalYm from Roche Pharma and Genentech, Inc. where she most recently was the Chief Quality Officer for Roche Pharma Technical Operations. In this role, she led a global team delivering end-to-end quality and compliance for Roche’s pharmaceutical commercial products and clinical pipeline. During this time, Andi was also a member of the Genentech, Inc. Executive Committee. Previously, Andi held various operational and executive roles in manufacturing, technology, and quality across Roche and Genentech. Andi holds a BA in Human Biology from Stanford University.