REGULATORY TOXICOLOGY EXPERT

About Us

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.

In a situation of non-stop growing demand, we’re working to build the best teams by inspiring, challenging and hiring the brightest talents from all over the World.

Mission

We are currently looking for an enthusiastic and motivated expert to join our multinational Toxicology Team. Ideally, you will have a background in PPP toxicology risk assessments, residues and study monitoring, with a broad understanding of the processes and procedures in the EU.

You will work closely with the Toxicology Team Leader and other Toxicology Experts. You will be responsible for delivery of Toxicology work, contributing to development of the teams skills and work scheduling.

The Toxicology team is responsible for performing Toxicology risk assessment for PPPs, Biocides and REACh sectors. This role is principally providing support for PPP regulations. You will need to work closely alongside our wider Plant Protection Team, or directly with the client’s team, who are responsible for the full dossier. A joined up and consistent approach is needed across all areas of expertise, so proactive communication and strong team working skills are essential.

Main Duties

• Drafting of Mammalian Toxicology sections of registration dossiers (PPP), including preparing study summaries and undertaking the risk assessment
• Present argumentation for waiving of certain studies where it is possible
• Design and study monitor appropriate mammalian toxicology studies (involving management of the studies delivered through CROs, budget responsibilities and contact with clients)
• Derive human health classification for substances and products according to the CLP Regulation
• Working as part of a multi-skilled project team, to develop robust documentation on behalf of the client
  
  

Profile

Essential

• Relevant scientific degree (e.g. Toxicology, Zoology, Pharmacology, Biology)
• At least 3 years practical experience in Regulatory Toxicology in the EU, either gained as consultant or regulator, or within industry
• Thorough working knowledge of the EU regulatory procedures for PPP is essential
• Ability to understand and accurately interpret data from studies in order to make appropriate scientific and regulatory conclusions and develop creative and practical solutions where possible
• Team player with strong decision-making skills, and keen to work in an international business environment
• Ability to work independently
• Have a good attention to detail
• Be a good communicator
• A high level of written and spoken English
  
  

Desirable

• Experience in study monitoring (e.g. acute toxicity data package, repeated toxicity studies)
• Experience with PPP Residues data packages (e.g. study monitoring, dossier writing, MRL calculations/applications, consumer risk assessments)
  
  

Permanent contract. This position can be office or home based.

Staphyt is present in many European countries.