An opportunity to join the EU Regulatory Affairs team at a global disinfectant products manufacturing company. You will work alongside an experience regulatory manager who will provide training where needed; your role will be to work on preparing dossiers for biocide products via the national/transitional notifications to EU countries.
This role will focus on dossier preparation for disinfectants (PT2, 3, 4 & 5); you will collate and review data, check the studies e.g. stability, efficacy, method of analysis etc, pull the dossier together and pass on to the partner organisation who will submit to the relevant country authority. You will focus on EU countries.
We are looking for someone with 1-2 years’ experience in regulatory affairs – ideally with biocides; experience of pulling together data for dossiers for other product types would also be of interest eg PPP (plant protection products), chemicals (REACH) and cosmetics (preparing PIFs) – this is not a role for a complete beginner – you must have some regulatory/dossier preparation experience.
Key Skills: Regulatory Affairs, biocides, regulatory submission, biocidal products, dossier preparation, data gathering, collation, compilation, national product notifications.
VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.