Mes compétences :
Agriculture
Agrochimie
Biologie
Écotoxicologie
Environnement
Homologation
Pesticides
Reglementation
Toxicologie
Veille
Gestion de projet
Entreprises
Arysta LifeScience
- Active Substance Registration Manager
NOGUERES2017 - maintenant
Adama France S.A.S
- Product Registration Manager
2016 - 2016
ISK Biosciences Europe N.V.
- Senior Registration Specialist
2015 - 2016I'm in charge of registration & regulatory affairs for active substances of our portfolio, including European processes & zonal ones for products. This includes registering substances according to Reg. 1107/2009 (new ones and renewals), registering new products or mixtures, label extensions etc.
This covers by extension all the contacts and exchanges with regulatory authorities, mainly in the Central zone where I'm accountable for Belgium, Czech Republic, Luxembourg, Hungary and Slovakia but also includes countries used as zRMS / RMS / coRMS in other regulatory zones.
In the mean time I'm in charge of study monitoring & risk assessments related to ecotoxicology, more focused on aquatic organisms and non target arthropods.
My responsibilities also cover CLP compliance and MSDS management.
ISK Biosciences Europe N.V.
- Registration Specialist
Project management: AIR dossiers, Annex III dossiers, monitoring of ecotoxicological studies & risk assessment for old & new active substances, C&L dossiers.
Country Management: Maintaining our portfolio & extending it in Belgium, Luxembourg, Czech Republic, Hungary, Croatia, Switzerland, Kenya, Israel and West Africa..
ISK BioSciences Europe N.V.
- Registration Assistant
Machelen2011 - 2012Registration of phytopharmaceutical products: herbicides, insecticides and fungicides.
Main task is the redaction of draft registration reports and monitoring of ecotox studies. Regulatory affairs & ecotoxicological risk assessment expertise are the two other key domains.
Global tasks include but are not limited to: Annex I listing of AI, zonal dossiers, national addendums & submissions.
I'm accountable for several central zone countries and for the ecotoxicological expertise for all dossiers.
2010 - 2010Prise en charge des dossiers de transformation d'AMMP en AMM, dossiers biologiques & toxicologiques; support aux équipes Registration & Development.
2010 - 2010Dans le cadre de mon stage de fin d'études, mes missions recouvrent, entre autres, les évolutions de la règlementation européenne et française dans le domaine de l'agrochimie, et plus spécifiquement, des produits phytopharmaceutiques ainsi que les différents procédés liés à leur homologation:
Veille technico-réglementaire, mise en place d’un outil de veille, gestion de bases de données, participation à la
réalisation de dossiers biologiques et toxicologiques, classification de produits formulés et soumission aux
autorités des dossiers correspondants, étude de la réglementation française et communautaire relative aux
produits phytopharmaceutiques :
Maîtrise globale du processus d’homologation des produits phytopharmaceutiques (Annexes II et III)
