We strengthen science together!
Present in Europe, North Africa, South America, STAPHYT brings together more than 600 employees, of different nationalities and cultures.
Rich in multiple profiles, a wide range of expertise is expressed in the Group, through our areas of activity which are agronomic experimentation, regulatory advice and coordination of registration files.
Staphyt’s Regulatory Affairs Division supports its clients in successfully bringing active substances and products to the market. We help clients understand and address the regulatory requirements for chemical or biological active substances and products in Plant Protection & Nutrition, Biocides and REACH sectors. Skills, experience and geographical coverage are three essential assets of our team to enable our clients to achieve their regulatory affairs objectives.
We are currently looking for an enthusiastic and motivated Ecotoxicologist to join our multinational and expanding Environment Team in Europe. Ideally, you have a strong background in environmental risk assessments and study monitoring in the area of Plant Protection Products.
You will be responsible for delivery of ecotoxicology work, contributing to development of the team’s skills and work scheduling. You will need to work closely alongside our wider Regulatory Team and/or directly with the client’s team. A joined up and consistent approach is needed across all areas of expertise, so proactive communication and strong team working skills are essential.

• Data Gap Analysis (DGA) including early phase testing strategy
• To present argumentation for waiving of certain studies where it is possible
• Design and study monitor of appropriate laboratory and field ecotoxicological studies (involving management of the studies delivered through CROs, budget responsibilities, contact with clients, etc.)
• Drafting of the Ecotox section of registration dossiers (also IUCLID format) and undertaking the risk assessment, including higher tier refinements
• Working as part of a multi-skilled project team, to develop robust documentation on behalf of the clients
• Providing strategic advice to clients and representing them in communication with Regulatory Authorities
• Various other tasks related to the registration of substances and products in Europe and the UK
• Appropriate peer review of other team member’s work