Sponsorship Portfolio
Two summits. One audience of senior life sciences manufacturing leaders from across North America.
Featured Speakers
Year after year, the portfolio brings life sciences manufacturing leaders from the world's largest organizations to the front of the room.
Eamonn Warren serves as Group Vice President of API and Dry Products Manufacturing at Eli Lilly and Company, where he leads the global network of internal and external manufacturing sites responsible for active pharmaceutical ingredients and dry-product production. He assumed this role in 2024 and is a member of Lilly’s Manufacturing Leadership Team.
Eamonn began his career with Lilly in 1995 at the Kinsale manufacturing site in Ireland as an automation engineer. Over the course of nearly three decades, he has held roles of increasing responsibility across engineering, operations, Six Sigma, human resources, and site leadership. His international experience includes assignments in Puerto Rico, Indianapolis, Augusta in the state of Georgia, and the Fegersheim manufacturing site in France.
Prior to his current position, Eamonn served as the global lead for Lilly’s Parenteral Manufacturing Network, where he oversaw strategy, performance, and modernization across Lilly’s sterile manufacturing capabilities. He is recognized for championing advanced and innovative manufacturing approaches as well as for his focus on operational excellence, talent development, and regulatory rigor.
A native of Ireland, Eamonn holds a degree in Chemical Engineering from University College Dublin and a degree in Management and Marketing from University College Cork.
Eamonn Warren
Group Vice President, Global API & Dry Products Manufacturing
Eli Lilly
Anne Kantardjieff, PhD, is Vice President and Head of CMC Development and Regulatory for Biologics and Advanced Therapies at Biogen. She is a seasoned biopharmaceutical executive with over 15 years of experience advancing complex biologics and cell and gene therapies from early development through global commercialization.
Anne is recognized across the industry for her expertise in CMC strategy, manufacturing scalability, and regulatory integration for advanced modalities. She leads global teams responsible for development, technical transfer, and regulatory CMC strategy across a diverse portfolio of biologics and ATMP programs, partnering closely with R&D, Quality, and Commercial Operations to enable reliable, inspection-ready supply and accelerated patient access.
Prior to Biogen, Anne served as Vice President of Manufacturing and MSAT at bluebird bio, where she led end-to-end supply and technical operations for four commercially approved autologous gene therapies—Zynteglo, Skysona, Abecma, and Lyfgenia. In this role, she oversaw external manufacturing partnerships, process validation, regulatory inspections, and commercial launch execution across multiple global markets.
Earlier in her career at bluebird bio, Anne drove strategic process improvements, expanded manufacturing capacity, and played a pivotal role in successful product approvals. She previously held leadership roles at Alexion Pharmaceuticals, where she led early- and late-stage process development teams and contributed to the commercialization of Strensiq, Kanuma, and Ultomiris.
Anne is known for building high-performing, collaborative organizations and integrating technical rigor with strategic decision-making to modernize manufacturing platforms and enable modality agility.
She holds a PhD in Chemical Engineering from the University of Minnesota and a Bachelor of Engineering in Chemical Engineering from McGill University. She is widely published and has held leadership roles within the American Chemical Society’s Biochemical Technology Division.
Anne Kantardjieff
VP, Head of CMC Development and Regulatory for Biologics and ATMPs
Biogen
Vinod Bulusu leads Products team in Global Technical Operations (GTO) and provides CMC leadership in Operations for Biologics modalities at AstraZeneca. Vinod, has about 20 years’ experience in commercializing biologics. Prior to AstraZeneca, Vinod worked at PwC as a management consultant and at Amgen led late stage process development and technology transfers. Vinod has a Masters in Chemical Engineering and an MBA.
Vinod Bulusu
Executive Director, Product Stewardship Lead
AstraZeneca
A chemical engineer by training with a Ph.D. in Chemical Engineering from The Technical University of Denmark, Hanne Bak started at Regeneron in 2004 as a Research Engineer in Preclinical Manufacturing and Process Development (PMPD). First, Hanne enjoyed increasing levels of responsibility within PMPD while also developing an Analytical team providing high throughput analytical support to PMPD. In 2015, Hanne transitioned into overall leadership of the PMPD department. In this role, she was responsible for all aspects of process development ranging from
molecule and cell line assessment and selection through technology transfer and post launch process optimization activities. Since joining Regeneron, Hanne and her team have been involved in the development and technology transfer of well over 100 novel manufacturing processes for mAbs, bispecifics, Adeno Associated Virus (AAV), Antibody Drug Conjugates (ADC), and Antibody Tethered Ligand (ALT) to eleven different Regeneron manufacturing suites, provided subject matter expertise for technology transfers to external contract manufacturing and partner sites, and contributed to or fully developed manufacturing processes for all of Regeneron’s thirteen (13) approved pharmaceutical drugs. Hanne has also overseen the digital transformation of PMPD, including extensive laboratory, process and data automation efforts and data architecture. In 2025, Hanne expanded her role to lead a newly formed function named Product, Analytical, and Process Development (PAPD), encompassing all aspects of process development through drug product, including extended analytical characterization, assay and reagent development supporting Regeneron from research through commercial manufacturing. Hanne is also the executive sponsor for Regeneron’s LGBTQ+ employee user group and serves on Regeneron’s Responsibility Committee.
Hanne Bak
Senior Vice President, Product, Analytical and Process Development
Regeneron
Jose Torres-Vorshirm is Senior Vice President of Global Technical Operations at BioNTech, where he oversees the end-to-end technical operations supporting the company’s pipeline and operations. His responsibilities encompass advancing a broad range of modalities—including antibodies and mRNA-based therapeutics—through development, manufacturing scale-up, and commercialization.
With more than 25 years of leadership experience in biopharmaceutical technical operations, global supply chain, and manufacturing, Jose has built expertise in delivering complex biologics and advanced therapies at commercial scale. Prior to his current role at BioNTech, he served in leadership roles at AstraZeneca, Eli Lilly and Company, and Novavax.
Jose holds a Master’s degree in Technical Management from Johns Hopkins University, a Postgraduate degree in Business Management and Supply Chain from the University of Warwick in England, and a Bachelor’s degree from the University of Puerto Rico-Mayaguez. He is a recognized leader in driving technical operations strategy and execution to bring innovative therapies to patients.
Jose Torres-Vorshirm
SVP Global Technical Operations
BioNTech
Laura Alquist joined Kite in 2016 and currently serves as Vice President and Global Head of Technical Operations.
She has more than 25 years of experience in all aspects of technical operations including manufacturing, supply chain, quality and information systems. Laura served as Vice President of Global Supply Chain at Kite before being named Global Head of Manufacturing in 2023. Under her leadership, Kite’s manufacturing team has improved its industry-leading track record for reliability and speed. Additionally, Laura successfully led the team in navigating the COVID-19 pandemic with zero supply disruptions to the patients and providers who rely on Kite’s therapies. Before joining Kite, Laura spent 20 years at Amgen in a range of global and operational roles of increasing responsibility across supply chain, manufacturing, quality and IT.
Laura holds a bachelor’s degree in business management from California Lutheran University and is APICS certified in supply chain operations.
Laura Alquist
Global Head of Technical Operations
Kite Pharma
Delegate Snapshot
A sample of the life sciences manufacturing leaders who attend across the portfolio. Every delegate is director level or above, vetted before they're seated.
Sr Director Supply Strategy
Vice President Quality Control
SVP, Head of Product Development & Clinical Supply
VP Global Quality
Executive Officer / Senior Vice President
Project Controls Director East Coast USA
SVP Americas Supply Operations
Senior VP, Manufacturing Operations
VP, Global Head of Platform Sciences
Chief Technical Officer
SVP, Quality & Regulatory
Director, Downstream Process Development
Director, Technical Services
Chief Technical Officer
Director, Gene Therapy Pilot Plant
Senior Vice President, Global Technical Operations and US Operations
Sponsor the Portfolio
Contact our team to learn more about sponsoring the full Life Sciences Manufacturing portfolio, one conversation, both summits, a year of access to senior life sciences manufacturing leaders.