People (List)
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Cecilia Turoff
Pfizer
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Sabrina Ullah
AtkinsRéalis
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Eva Urban
CSL Behring
Eva M. Urban, currently Director at CSL Behring, leads the Global Internal Audits & Compliance team. She has 30 years’ experience in various roles – quality and operations and R&D - in Biopharma (Lonza, Celgene, CSL). Areas of expertise are Risk Management and Quality Systems including design and implementation locally and globally, Leading Internal Auditing and Hosting Regulatory Inspections, Quality Operations, Biotech R&D, Biopharmaceutical API (DS) Manufacturing, Aseptic Processing, External Vendor Quality Oversight. -
Robin Usselman
ACIC Machinery
Robin Usselman is a Business Development Manager at ACIC Machinery where she collaborates with manufacturers to provide specialized equipment such as automatic inspection machines and custom automation. This role has provided her with an opportunity to work with industries including pharmaceuticals, biotechnology, and radiopharmaceuticals. -
Frédéric Vacher
Frédéric is technologist in the Analytical Sciences department of Sanofi Pasteur. With +20 years of experience in microbiology, he has a strong background in endotoxin testing. As an internal technical endotoxin SME, Frédéric participates to complex troubleshooting, screening, and implementation of new technologies. -
Kristin Valente, PhD
Merck & Co., Inc.
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Rosmy Carolina Valoyes
Head of Corporate Quality Systems, Boehringer Ingelheim
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Erik van Asselt
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Martin VanTrieste
Martin VanTrieste is the CEO of Civica Rx who was recently named a “Champion of Change” on The Medicine Maker’s Power List for his role in leading Civica, a new, nonprofit enterprise created to stabilize the supply of essential generic medications. Martin brings over 36 years in the industry, with comprehensive experience in biopharmaceutical manufacturing, quality systems and related government regulations in the US and around the world. -
Kaitlyn Vap
Veolia Water Technologies & Solutions
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Romain Veillon
Romain Veillon is Senior Manager Visual Inspection & Leak Testing at GSK Vaccines, in Global MSAT Manufacturing Technologies. As global expert he is leading Visual Inspection performance and expertise network on multiple sites. -
Jackie Veivia-Panter
BioCentriq
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Romain Vellion
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James L. Vesper
"Root Cause Investigations for CAPA: Clear and Simple"
James Vesper, Ph.D., MPH, has worked in the pharma/biopharma industry for more than 35 years, starting out at Eli Lilly and Company where his last position was leading Lilly's GMP Training and Education group. For 24 years, he was President of Learning Plus, a consultancy that provided training and performance solutions to the pharma and biopharma industry. In 2017, he joined ValSource as Director of Learning Solutions. His professional interests are in the areas of learning/education, learning course design, risk management, and incident investigations related to the category of "human error." -
Friedrich von Wintzingerode, PhD
Vice-Chair, Roche
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Elisabeth Wagner, CSL Behring
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Kelly Waldron, PhD
Valsource, LLC
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Karen M. Walker
BioAB Vice-Chair
Karen Walker, Sr. Advisor Cell and Gene Therapy Manufacturing at Roche/GNE. Karen brings >30 years’ experience in the biotech industry, holding positions in Technical Development, Regulatory Affairs and Quality. She has worked in a number of companies including Seattle Genetics, Novartis, Amgen, Bayer, and several other small to mid-sized biotech companies. -
Bonnie Ward
President & CEO, Quality Compliance Partners, Inc.
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Brent Watkins
Veltek