Description

With over 15 years of experience as a Biological Engineer and Lab Manager, I partner with biotech, pharma, and food-tech companies to structure, optimize, and scale their R&D operations.

My approach balances scientific rigor with operational pragmatism. I do not just manage projects; I transform complex technical challenges into streamlined, compliant, and high-performing processes.

Domaines d’expertise

Langues

Français
Bilingue ou natif
Anglais
Capacité professionnelle complète

Préférences en matière de lieu de travail

Accepte de travailler sur site

Paris (jusqu’à 50 km)

AB Science
Project Manager
INDUSTRIE PHARMACEUTIQUE
mars 2016 - juin 2024 (8 ans et 3 mois)
Évry, France
• Establishment and development of the AB Science R&D branch at Genopole
• Management of projects in immuno-oncology and neurology: development of therapeutics vaccines (viral particles) and small molecule testing in cancer and ALS (tyrosine kinase inhibitors)
• Recruitment and management of operational staff
• Reporting and presentation of results to the various chemistry/biology teams with teaching methods
• Implementation and monitoring of the quality system (SOP, ELN/LIMS, method validation)
• Scientific monitoring and technological innovation. Data analysis for publication and patent
R&D Project Management Gestion de projet Management d'équipe Système qualité Innovation
Faircraft–
Laboratory Manager
BIOTECHNOLOGIES
novembre 2024 - août 2025 (9 mois)
Paris, France
• Supervision of a team of technicians and engineers for R&D activities for in-vitro leather
• Organization, project planning and daily management of the laboratory (production and QC tests).
• Recruitment, integration, continuing training and conducting annual interviews. Hygiene and safety manager for laboratories and operations (16 people)
• Management of service providers and suppliers (negotiation, partnership, etc.)
Hygiène et sécurité Laboratory Management R&D Project Management Recrutement Négociation et Gestion des Fournisseurs
Theravectys–
Process Dev. Engineer
BIOTECHNOLOGIES
janvier 2013 - janvier 2016 (3 ans)
94800 Villejuif, France
• Development of USP/DSP processes for the production of lentiviral vectors.
• Scale transfer 1L → 20L GMP with complete drafting of quality documents.
• Training of engineers and drafting of SOPs for production and purification.
• Validation of QC methods: qPCR titration, FACS, ex-vivo toxicity
DSP USP Lentivirus Method Validation Technology Transfer