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Arnaud MULLER

DIDENHEIM

En résumé

Since January 2017:
Laboratory chief at Hoffmann-La Roche Basel in PTDC-A, Section QC-DP ( small molecule analytical development, cGMP Procedures)
Organisation of the laboratory’s activities
Coordination of the analyses
Reviewer function for the documentation and in BALI system
Analyses for customers (galenic development, analytical development groups - late stage and early stage)
Analytical methods handover and implementation

Mes compétences :
wastes' management
Quality Control
Pharmacokinetics
Microsoft Word
Microsoft Excel
Histology

Entreprises

  • Hoffmann-La Roche - Senior Associate

    2011 - 2016 "Senior Associate'' at Hoffmann-La Roche Basel in PTDCD (analytical development, cGMP Procedures)

  • Hoffmann-La Roche - Laborspezialist

    2011 - 2011 "jobrotation'' at Hoffmann-La Roche in PTDA (analytical development for Drug Substances, cGMP Procedures)

  • Hoffmann-La Roche - Laborspezialist

    2007 - 2008 "new perspective'' at Hoffmann-La Roche in PTDFP (packaging development, cGMP Procedures)

  • Hoffmann-La Roche - Laborspezialist

    2006 - 2006 For one year (in 2006 ) : work experience in "Hochaktiv Labor'' of PTDFA with a substance
    category 4, from analyse to wastes' management ,

  • Hoffmann-La Roche - Laborspezialist

    2003 - 2011 "Laborspezialist'' at Hoffmann-La Roche Basel in PTDFA (analytical development, cGMP Procedures)

Formations

  • University Louis Pasteur

    Strasbourg 2001 - 2003 Master Sciences of drugs

    Master 2 - Analysis, Registration and Production of Drug:
    - September 2001 - March 2002: training period in Therapeutic Chemistry Laboratory (absorption's pharmacokinetic studies with everted intestinal sac from rats; histology and liquid chromatography)
    - April 2002- March 2003: work experience at Hoffmann-La Roche Ltd into PRNS Basel (distribution's pharmacokinetic in vitro studies, detection

  • Novartis Pharma AG

    Huningue 2000 - 2001 professional experience

    work experience in analysis laboratory, Quality Control (with GLP procedures), sector Finished Product:
    - Analysis of finished product at time 0 (liquid chromatography with UV detection)
    - Stability tests, performance qualification (procedure of validation of fabrication)

  • University Louis Pasteur

    Strasbourg 1998 - 2000 Master 1 (in biochemistry)

  • University Louis Pasteur

    Strasbourg 1997 - 1998 Bachelors Degree (in biochemistry)

  • University Louis Pasteur

    Strasbourg 1996 - 1997 DEUG (in biology)

  • Medecine University

    Strasbourg 1994 - 1996 first cycle

  • Academy Of Strasbourg

    Mulhouse 1993 - 1994 baccalauréat C

Réseau

Annuaire des membres :