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Alain LAMPROYE

NANCY

En résumé

Mes compétences :
General Management
Project Management
maintenance
covering purification development
Standard Operating Procedure
Quality Control
Management Training
Logistics
Journals
Iteral Management
Intellectual Property Law
Immunoassay
HPLC
ELISA
Communications

Entreprises

  • Novasep Group - President, Biopharma Business Unit

    2013 - maintenant NOVASEP

    Novasep Group
    39, rue Saint-Jean-de-Dieu
    F-69007 Lyon, France


    President, Biopharma Business Unit

    * General Management of the Biopharma Business Unit (280 employees), annual turnover 60 M EUR ;
    * Board member of the Executive Committee of Novasep ;
  • NOVASEP - Chief Executive Officer

    POMPEY 2012 - 2012 Novasep Belgium
    Avenue des Professeurs Jeener et Brachet
    B-6081 Gosselies, Belgique

    Chief Executive Officer

    * General Management of Contract Manufacturing Organization (100 employees), specialized in the production of viral vectors and recombinant proteins for therapeutic use. ;
    * Board member of Novasep Process Division ;
  • Microbial Technologies - Director

    2011 - 2012 MERCK SERONO

    MerckSerono BioDevelopment
    1, Rue Nicolas Brémontier
    F-33650 Martillac, France

    Director, Microbial Technologies

    * Management of an investment project into a new GMP manufacturing facility for microbial-based products (14.1 mio EUR investment) ;
    * Responsible for process technical transfers from CMOs ;
  • EMD Serono Biotech Center - Site Director

    2009 - 2011 EMD SERONO

    EMD Serono Biotech Center
    Middlesex Turnpike 45A
    Billerica, MA01821 - USA

    Site Director

    * General management of EMD Serono Biotech Center (57 persons), part of the Technical Operations division of MerckSerono.
    * Responsible for the supply of preclinical and clinical GMP materials, up to Phase 2 ;
  • Merck Serono Biotech Center - Associate Director & Deputy Director of the Biotech Process Development Department

    2006 - 2009 MERCK SERONO
    Merck Serono Biotech Center
    Zone Industrielle B
    CH-1809 Fenil s/Corsier - Switzerland

    Associate Director

    * Deputy Director of the Biotech Process Development Department (62 persons). Responsible of process development activities, covering upstream, downstream and analytical activities. Development of production processes for recombinant proteins, expressed in mammalian cell culture. ;
  • Laboratoires SERONO S.A. - Downstream Group Manager

    2003 - 2006 Serono Biotech Center
    Zone Industrielle B
    CH-1809 Fenil s/Corsier - Switzerland


    Downstream Group Manager

    * Head of the downstream development group (20 persons): activities covering purification development of recombinant proteins, process scale-up and validation, improvement and troubleshooting of manufacturing processes.
    * Project management: leading the Phase 2/3 process development of recombinant proteins. ;
  • EUROGENTEC s.a. - GMP Production Director

    1999 - 2003 Eurogentec is a CRO/CMO working as subcontractor for pharmaceutical industries and providing development and production capacities of recombinant proteins and DNA. Clinical batches of recombinant proteins are regularly produced for phase 1 and 2 clinical trials.

    * Management of the pharmaceutical production units (fermentation, purification, QC, maintenance and logistics teams - 30 people).
    * Project management from the development phase (R&D) of processes to their transfer to the GMP production unit (production of recombinant proteins and DNA). ;
  • PHAROS s.a. - R&D Downstream Manager

    1996 - 1999 * In charge of the development and the scaling-up of purification methods for a recombinant protein. This work was realized in the scope of the exclusive sub-contracting agreement between SmithKline Beecham Biologicals and Pharos. ;
  • PHAROS s.a. - Research scientist

    1989 - 1996 * Laboratory of biochemistry : HPLC, protein purifications, immunoassay (RIA, RRA, ELISA), electrophoresis, micro and ultrafiltration. ;
    * Writing of standard operating procedures (SOP), analytical method validation, quality control of a recombinant protein. Set-up of Good Laboratory Practices (GLP) in the laboratory.
    * Work in a pharmaceutical Production Unit, following the Good Manufacturing Practices (GMP) ;
  • UNIVERSITY OF LIEGE - Assistant

    1984 - 1989

Formations

  • University Of Liège (Belgium) (Liège)

    Liège 1980 - 1984 M. Sc. Biology
  • University Of Liège (Belgium) (Liège)

    Liège 1980 - 1984 M. Sc. Biology

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