À propos de Sébastien
Français
Bilingue ou natif
Anglais
Capacité professionnelle complète
Expériences
- FreelanceConsultantoctobre 2024 - Aujourd'hui (1 an et 8 mois)Mission:• Support development of analytical methods to quantify chemical in biological fluids.• Support to ADME characterization for topical productsAchievements:• Transfer of in silico model dedicated to cutaneous absorption• Development of an exposure model to volatile chemicals• Mass spectrometry training for quantification of proteins.
- L'Oréal, Aulnay sous Bois (Cosmetic)Senior Research AssociateCENTRES DE RECHERCHEavril 2003 - septembre 2024 (21 ans et 5 mois)Mission:• Support conception and development of new safe and performant cosmetics products (raw material and formulation) through their ADME properties• L'Oréal representative at Cosmetic Europe : Development and advocacy of alternative methods to animal testing : local tolerance (sensitization) and systemic toxicity (LRSS and ICCS programs)Achievements:• Development of LC/MS and GC/MS methods for quantitative and qualitative analysis (small chemicals, vegetal extracts, peptides, proteins,…)• Development of LC/MS methods on Q-exactive system for metabolites and degradation products identification• Development of ADME methods dedicated to cosmetics raw materials• Development of methods for skin absorption using different membranes (ex vivo skin, reconstructed skin, synthetic membranes,…)• Development of methods dedicated to skin imaging (CARS, MALDI, SIMS)• Development and validation of skin absorption QSAR models• Deployment aux PBPK approaches for cosmetic applications• Development and set up of in vivo protocol to measure skin absorption• Setup a CRO network (Aliri, Eurofins, Pharmacelsus, Biogalenys, Biomeca,…)• Support brands for claim• Team management (4 people)
- (Pfizer, Synthelabo, Innothera, Rhône-Poulenc, Aralco, Servier)Research ScientistCENTRES DE RECHERCHEseptembre 1997 - avril 2003 (5 ans et 7 mois)• Development of high throughput analytical method with one sample analyzed every 25 seconds• Development and validation of an analytical method to characterize a drug counterfeit through synthetic impurities using a first-generation LC-ToF.• Set up of LC/MS/MS activities for ADME, metabolites identification and quantitative analysis in biological fluid.• Development and validation of an analytical method by LC/MS/MS for quantitative analysis of plasma samples dedicated to GLP studies (pre-clinical, Phase 1 et Phase 2)• Set up of ISO9001 quality system for GC/MS activity dedicated to flood favor characterization• Development of GC/MS and LC/MS activities for synthetic impurities characterization in pre clinical and clinical batches
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