Team
Committee of Experts at the European Biotech Venture Builder
María Sola Gil
Professional Profile
María is a biotechnology, pharmaceutical, and healthcare professional with over 15 years of experience building global innovation teams and managing strategic portfolios from inception through commercialization. She has developed valuable ecosystem connections, achieved successful commercialization of high-risk ventures, and gained entrepreneurial experience as founder and promoter of healthcare ventures.
She is also a recognized domain expert, having participated as keynote speaker in international congresses and events, served as advisor to European innovation and government initiatives, and is a visiting professor in innovation management programs at European universities.
Karl Schmieder
Professional Profile
Karl helps life sciences companies develop strategies to grow and succeed. He has done so for dozens of companies that have raised millions and sold billions of dollars in products.
He works with executives to develop thought leadership programs, create engaging content, and position them as influencers driving the biotech and synthetic biology industries forward.
He is also the co-author of What’s Your Bio Strategy? — a book exploring the impact of synthetic biology and gene editing on business. He has presented its topics on four continents and in two languages.
Karl teaches Fortune 1000 companies, associations, and students how to develop strategies that integrate engineered biology.
How will you use biology to differentiate your business?
He is passionate about biotechnology and excels at translating complex science into compelling stories — stories that have led to hundreds of millions of dollars in investment, sales, and publicity. He has helped launch blockbusters like Risperdal (Janssen), Lucentis (Genentech), Januvia (Merck), and was an early advisor on science storytelling and thought leadership to K18Hair.
Alastair Waugh
Professional Profile
Alastair has over 15 years’ experience in industrial and regulated biopharmaceutical production from CDMOs, having worked at Lonza Biologics (Slough), SynCoBio Partners (Amsterdam) and 3P Biopharmaceuticals (Pamplona). Prior to industry, Alastair had an academic career focused on protein biochemistry, working within cancer biology and antibiotic biosynthesis fields. Currently, Alastair works as an independent consultant at CQA Bio Consulting, supporting biologic and CGT CMC product development for an international client base.
Alastair has found himself as a guardian of product quality, working at the interface between bioproduction and analytics. At 3P Biopharmaceuticals, he established and led a large Analytical Development group, who, together with leaders in Process Development, worked on a broad variety of microbial and mammalian protein biologics, from pre-clinical to commercial, encompassing peptides, growth factors, vaccines, pegylated proteins, mAbs, ADCs, VLPs, etc. Notably, Alastair was a key player in 3P’s role in developing and manufacturing a pegfilgrastim biosimilar (PELMEG®), the first authorised biosimilar in Spain.
Currently, he brings his expertise to companies such as BioNTech, Polpharma, Xalud, Nordic Nanovector, Mannin and VIVEBiotech.
Karsten Dörr
Professional Profile
Karsten is a senior executive with more than 35 years of expertise in global quality management, quality assurance, quality control and compliance, with a proven record in leading international teams and implementing strategic concepts. A well-versed, internationally recognized expert in global compliance with a strong background in communication and negotiation. His expertise has been previously implemented in big pharma companies, as well as CMOs and biotech firms.
César de la Fuente
Professional Profile
César de la Fuente is a Presidential Associate Professor at the University of Pennsylvania, where he leads the Machine Biology Group. He completed postdoctoral research at MIT and earned a PhD from the University of British Columbia (UBC). His research goal is to use the power of machines to accelerate discoveries in biology and medicine.
Notably, he pioneered the development of the first computer-designed antibiotic with efficacy in animal models, demonstrating the application of AI for antibiotic discovery and helping launch this emerging field. His lab is at the forefront of developing computational methods to mine the world’s biological information, leading to the identification of over a million new antimicrobial compounds. These efforts began by exploring the human proteome as a source of antibiotics for the first time.
His team was also the first to find therapeutic molecules in extinct organisms, launching the field of molecular de-extinction, which has already yielded preclinical antibiotic candidates such as neanderthalin, mammuthusin, and elephasin.
De la Fuente’s lab has expanded its antibiotic discovery efforts to explore microbial dark matter, identifying nearly one million new antibiotic molecules, which have been made freely available and open access to encourage global research collaboration. This work leveraged machine learning to analyze 63,410 metagenomes and 87,920 microbial genomes.
Additionally, by exploring thousands of human microbiomes, the team discovered new antimicrobial agents, including prevotellin-2 from the gut microbe Prevotella copri. Collectively, these efforts have reduced the time to identify preclinical antibiotic candidates from years to just a few hours.
Further advances include:
Reprogramming venoms into antimicrobials
Developing autonomous nanorobots to treat infections
Creating resistance-proof antimicrobial materials
Inventing rapid, low-cost diagnostic devices for COVID-19 and other infections
Prof. de la Fuente is an NIH MIRA investigator and has received over 80 national and international awards. He is an elected Fellow of the American Institute for Medical and Biological Engineering (AIMBE), one of the youngest ever inducted.
He has been recognized by MIT Technology Review as one of the world’s top innovators for “digitizing evolution to make better antibiotics,” and has received numerous prestigious honors, including:
The Langer Prize
ACS Kavli Emerging Leader in Chemistry
ASM Distinguished Lecturer
Miklós Bodanszky Award
AIChE’s 35 Under 35 Award
Princess of Girona Prize
National Academy of Medicine Emerging Leader in Health and Medicine, among many others
He serves on the editorial boards of top journals and is Associate Editor of Drug Resistance Updates (IF = 24.3), Nature Communications Biology, Bioactive Materials, and others. He has been named a Highly Cited Researcher by Clarivate multiple times.
Prof. de la Fuente has delivered over 300 invited lectures, including Keynotes, Named Lectures, and TEDx, and is co-author of an influential book on machine learning for drug discovery, with multiple patents and over 160 peer-reviewed publications in top-tier journals such as Cell, Science, Nature Biomedical Engineering, and PNAS.
Dr. Christopher Marquis
Professional Profile
Dr. Christopher Marquis is a biochemical engineer with expertise in fermentation, cell culture, recombinant proteins, and downstream processing. He is an Associate Professor at the School of Biotechnology and Biomolecular Sciences, University of New South Wales (UNSW), Sydney, Australia.
He has a strong track record in collaborative research and industry engagement in biotechnology, particularly at the interface between chemical engineering and biology.
Dr. Marquis established the UNSW Recombinant Products Facility (RPF), which provides services and infrastructure to academia and industry in protein production, purification, and characterisation. The facility also delivers training and access to these capabilities for UNSW students and staff, along with fee-for-service operations.
In this role, Dr. Marquis has overseen the production and purification of dozens of proteins for research purposes, including two proteins for first-in-man Phase I clinical trials. In 2021, he led the ISO9001 accreditation of the facility, and he also established plasmid manufacturing capacity as part of the UNSW RNA Accelerator Program.
In addition to running the RPF, Dr. Marquis has a productive research career with over 80 co-authored publications and numerous research collaborations with academic groups and industry. He is an invited reviewer for several scientific journals and a grant reviewer for the Australian Research Council. He is also a member of the NSW committee for AusBiotech, the national liaison body for biotechnology in Australia, through which he maintains extensive industry contacts.
Dr. Dieter Braun
Professional Profile
Dieter is a professional Global commercial thinker with P&L understanding and more than 25 years of experience in small biotech and big pharma companies across multiple countries and regions.
Broad expertise across the pharmaceutical value chain, including strategy, portfolio management, R&D, business development & licensing, commercial operations, and manufacturing
Expert in building commercial infrastructure from scratch and generating revenue through heterogeneous sales channels such as retail, hospital, OTC, and SHI tendering
Skilled in launching and acquiring products across Europe, identifying opportunities via licensing or co-marketing, while effectively balancing risks to drive sustainable growth
Strong international experience collaborating with headquarters, sales organizations, business partners, and alliance management across Europe, the US, and RoW
Positive, hands-on, entrepreneurial, and charismatic leader with out-of-the-box thinking, who inspires teams and promotes a can-do attitude to drive projects and achieve KPIs and deliverables
Barbara Gastl
Professional Profile
Barbara has more than 20 years of experience in clinical operations. Having managed global clinical trials across all phases and various therapeutic areas, she now works as a consultant on all aspects of clinical operations and compliance. Her focus lies in quality management system development and training.
Sergio Martínez Pérez de Albéniz
Professional Profile
As the Finance Representative, Sergio holds a double degree in Business Management and Administration and Law from the Public University of Navarra, with a master’s degree in International Trade from Menéndez Pelayo University in Madrid. He has more than 10 years of experience, both nationally and internationally, working with institutions such as the Spanish Economic and Commercial Office in Los Angeles and the Spanish Consulate in New York. He has also managed various private companies, specializing in pharma/biotech start-ups, where he led their equity strategies, investment rounds, and funds deployment, among other financial responsibilities.