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SOLVAY (ex-Rhodia)
- Regulatory Toxicologist
Courbevoie
2010 - maintenant
- Preparation of expert regulatory documentation to support REACH submissions (datagap analysis, data evaluation and insertion in IUCLID database, establishment of DNELs, Chemical Safety Assessment and Chemical Safety Report)
- Preparation of toxicological profiles and risk assessments based on experimental and/or literature data
- Design and monitoring of in vivo and in vitro toxicology studies conducted in CROs (acute and subchronic systemic toxicology, eye and skin corrosion/irritation, skin sensitization, genetic toxicology, reproductive toxicology)
- Classification of substances according to CLP (Classification Labelling Packaging) and GHS (Globally Harmonized System) regulations
- Preparation of Safety Data Sheets according to the GHS and REACH legislation
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MDS Pharma Services
- Study Director in Toxicology
2007 - 2010
Study plan design and writing, monitoring of the in-life phase, data interpretation and reporting of general toxicology studies (local tolerance, dose range finding, juvenile, 1- to 6-month toxicity studies; rodent (rat, mouse) and non-rodent (monkey, dog and rabbit)
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Pfizer Global R&D
- Scientist in clinical pathology
Paris
2006 - 2007
Interpretation and reporting of hematology and clinical chemistry data (in vivo toleration/range-finding/escalating dose and exploratory studies; 2 weeks to 1 month toxicity studies)
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Pfizer Global R&D
- Scientist in molecular and cellular toxicology
Paris
2005 - 2006
- Protocol writing, data interpretation and reporting of toxicogenomics studies
- Literature search
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Pfizer Global R&D
- Laboratory technician in Molecular and cellular toxicology
Paris
1998 - 2005
- Performing toxicogenomics studies (Microarray and real-time RT-PCR)
- Performing and validating in vitro models for the irritancy potential evaluation of molecules in development
