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.

Industry field of expertise

Languages

French
Native or bilingual
English
Fluent

Workplace preferences

Can work on-site

Paris (up to 50km)

AB Science
Project Manager
PHARMACEUTICALS INDUSTRY
March 2016 - June 2024 (8 years and 3 months)
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
BIOTECH
November 2024 - August 2025 (9 months)
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
BIOTECH
January 2013 - January 2016 (3 years)
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