Regulatory toxicology expert H/F

at  STAPHYT

London, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate20 Jan, 2025Not Specified21 Oct, 20243 year(s) or aboveGood communication skillsNoNo
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Description:

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 team’s 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.

Responsibilities:

  • 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


REQUIREMENT SUMMARY

Min:3.0Max:8.0 year(s)

Information Technology/IT

Software Engineering

Graduate

Proficient

1

London, United Kingdom