UNIVERCELLS
Nicolas Moniotte currently serves as CTO and Head of Development at Quantoom Biosciences and VP R&D at UNIVERCELLS. Extensive experience includes roles such as Co-Founder and CTO at Dillico, Consultant for mRNA Vaccine Technology Transfer at CureVac, and Chief Technology Officer at Magnetrap sa. Prior experience at GSK spanned over a decade, with key positions including Director of Acceleration of Vaccines Development and Director of Analytical Development, leading efforts in vaccine R&D and analytical strategies. Educational qualifications include a PhD in Chemistry from Université de Namur and a Business Analytics certification from Wharton Online.
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UNIVERCELLS
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Univercells is a global life sciences company making biologics available to everyone. We operate as a campus of start-ups: five businesses solving different parts of the same puzzle - meeting global demand for bioproduction. Because it is not enough for a drug to exist. To change the world it must be accessible to everyone. Each division of affiliates operates a different part of the healthcare value chain, through a distinct business model: Exothera is a Contract Manufacturing and Development Organization (CDMO) for biologicals, mainly vaccines and viral vectors, with GMP production facilities in Belgium and offering process development and optimization services. https://exothera.world/. Unizima delivers international project management of technology transfer, alongside operational support services (quality, supply chain, digital) and bioproduction training programs, as well as care centers and diagnostics surveillance centers. https://unizima.com/. At Quantoom Biosciences, scientists, engineers and clinicians are committed to solve some of the biggest challenges facing mRNA-based vaccines and therapeutics by developing an end-to-end RNA Platform. This includes DNA and RNA manufacturing and formulation, along with critical reagent supply, from sequence to large-scale production. https://www.quantoom.com/. Thanks to a substantial knowledge of the pharmaceutical industry and a strong scientific background, RLM Consulting provides international regulatory affairs support at all stages of product development, from discovery research through preclinical and clinical testing, up to and beyond submission of the dossier for marketing authorization. http://www.rlmconsulting.be/.