QUALITY ASSISTANCE S.A.
Vincent Van Mullem has extensive work experience in the scientific field. Vincent began their career as a Ph.D. candidate in Molecular Biology, focusing on transcription regulation in Saccharomyces cerevisiae at CEA and FUNDP. After completing their Ph.D., they worked as a Postdoc at FUNDP, studying protein-protein interactions in Brucella melitensis. Van Mullem then moved on to a Postdoc position at CEA and FUNDP, conducting research on transcription elongation in Saccharomyces cerevisiae.
In 2003, Van Mullem joined Quality Assistance as a Microbiology Lab Manager, responsible for managing projects and overseeing the microbiology lab. Vincent later took on the role of Biology & Biotechnology Lab Manager, where they were responsible for project timelines, budgets, and method development. Vincent then progressed to the positions of Scientific Director and Operations Director, overseeing analytical units and coordinating teams. Finally, they became the Scientific Operations Director, heading the Biology and Physicochemistry departments.
Throughout their career, Van Mullem has published scientific articles in reputable journals such as EMBO J. and Proc Natl Acad Sci U S A, showcasing their expertise and contributions to the field.
Vincent Van Mullem has a PhD in Molecular Biology from Facultés Universitaires Notre-Dame de la Paix in Namur, Belgium, which they completed in 2001. Their research focused on transcription regulation in Saccharomyces cerevisiae. Prior to their PhD, they obtained a Master of Science (DEA) in Genetics from CEA in Saclay, France in 1997. In 1996, they completed their Bachelor of Science (B.Sc.) in Molecular Biology from Facultés Universitaires Notre-Dame de la Paix in Namur, Belgium.
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QUALITY ASSISTANCE S.A.
Quality Assistance S.A. is a leading European Contract Research Organisation (CRO) providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products. We assist our clients through non-clinical and clinical studies to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences. For each client project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs. Quality Assistance S.A. is an expert for the development of : - Biotherapeutics, monoclonal antibodies, ADCs - New Chemical Entities, peptides, oligonucleotides - mRNA - Viral vectors - Vaccines - Cell-Based Medicinal Products - Nanomedicines The company holds a unique position on the market with : - all its laboratories on one site : Bioanalysis, Bioassays, Biochemistry, Chromatography, Elemental Impurities, Mass Spectrometry, Microbiology, Molecular Biology, Protein Characterisation - 250 highly qualified professionals - over 40 years’ expertise at the forefront of analytical sciences. The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant. Visit www.quality-assistance.com to learn more about our expertise and analytical services.