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Experiences

Current Experience

  • Process improvement Manager/Scientist for GSK


    Since October 2013
    at gsk' i'm working as a support for 2 buildings of production and my mission is to implement a new single use technology into viral and vaccine processes, in collaboration with denmark and us. Project Management & Scientist activities as: - constitution of a project team - coordination of the project between belgium, us and denmark - strong interactions with legal, Intellectual Property and financial stakeholders - coordination of activities between production and R&D services onsite - management and installation of a new Laboratory onsite and lead of experiments (orders, Supply Chain, coordination) - Training and supervising new team members or more junior staff - Planning, carrying out and supervising process trials at small scale; - write test protocols/reports, procedures, SOP’s, urs, risk assessments - Validation of single use technologies - evaluate existing processes to identify areas for improvement - support in defining critical process parameters, set specification and control to ensure quality is maintained - generating data to demonstrate comparability, safety and efficacy of the products in consultation with other functions, - improving yields by reducing costs At GSK' I'm working as a support for 2 buildings of production and my mission is to implement a new single use technology into Viral and vaccine processes, in collaboration with Denmark and US. Project management & scientist activities as: - Constitution of a project team - Coordination of the project between Belgium, US and Denmark - Strong interactions with legal, intellectual property and financial stakeholders - Coordination of activities between Production and R&D services onsite - Management and installation of a new laboratory onsite and lead of experiments (Orders, supply chain, coordination) - Training and supervising new team members or more junior staff - Planning, carrying out and supervising process trials at small scale; - Write test protocols/reports, procedures, SOP’s, URS, risk assessments - Validation of single use technologies - Evaluate existing processes to identify areas for improvement - Support in defining critical process parameters, set specification and control to ensure quality is maintained - Generating data to demonstrate comparability, safety and efficacy of the products in consultation with other functions, - Improving yields by reducing costs

Past Experience

  • Process Development Scientist, Bioprocess R&D Department, Upstream platform

    March 2012 --- August 2013
    management of project: - supported, developed and implemented novel technologies for a transition between phases 1 & 2 of a vaccine - managed a transfer of a technique between 2 different countries - managed a schedule, delays and counstraints - interacted with internal and external collaborators Process development: - developed a new Cell line for High Throughput Screening of supplements (transfections, cloning, Cell banking) - optimized a serum free culture medium for DNA-Virus production within vero cells on microcarriers - executed small and medium scale experiments in shake flasks, spinners and bioreactors up to 50l (millipore, dasgip) analytical: - plaque assay analytical technique

  • Internship Sanofi Pasteur -Bioprocessing R&D Dpt, Upstream platform-

    January 2011 --- December 2011
    management of project: - developed a rt-qPCR, generating my own samples in bioreactors - planned and scheduled the experiments - respected deadlines - negociated with internal and external collaborators and suppliers - presented results Process development: - optimized a serum free culture medium for rabies Virus production within vero cells - cultured and infected cells on microcarriers in different bioreactors up to 8l - assessed a new model Lab scale single use bioreactor for Process development analytical: - developed a rt-qPCR in process monitoring tool - analyzed Gene expression - worked on RNA chips

  • Internship MERIAL; BioAnalytical Development Dept - PCR platform

    January 2010 --- September 2010
    analytical: - developed of a qPCR that replaced the reference analytical technique for canarypox Virus Titration on cells (dicc50) - cloning, DNA/arn isolation (manual, in plates) - ccid50 technique quality - editited procedures - stability studies - validated a technique - redacted Validation, correlation and stability reports additional - trained and qualified technicians - worked in p2 environment

Knowledge

LinkedIn Assessment :
BiotechnologyCell Culturemolecular biologyMammalian Cell CultureVirologyBioreactordisposable bioreactorBioprocess DevelopmentVaccinesUpstream processingMultiplex PCRPCR primer designCloningBioprocessingR&D

Education

  • Master R&D Biotechs in Biotechnologies from Université Pierre et Marie Curie (Paris VI) in 2011
  • ESSEP 3 in Biotechnologies from Université catholique de Lyon in 2010
  • licence in Biologie Cellulaire et Physiologie from Université Jean Monnet Saint-Etienne in 2009

Area / Region

Belgique

Others

Driving License
  • No

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