**1.1 聽 聽Job Objective聽**
Provide guidance, expertise and support to the team regarding 聽preparation of the toxicological sections of registration dossiers for active ingredients and formulated 聽products regulated under the Regulation (EC) No 1107/2009 of the European Parliament and of the 聽Council of 21 October 2009 concerning the placing of plant protection products on the market. These tasks will be undertaken in order to achieve the business鈥檚 agreed strategic, financial and 聽quality objectives聽
1.2 聽Key tasks
(a) 聽Evaluate client data under the focus of regulatory requirements for toxicological data (Data 聽Gap Analyses, Risk Assessments, Exposure Estimates, Product Classification)
(b) 聽Develop of strategies to assist clients in experimental programs according to European, 聽international and national data requirements
(c) 聽Summarise experimental data for authorisation including judgement of experimental work with 聽regard to satisfying the quality and focus to fulfil the regulatory requirements聽
(d) 聽Prepare of risk assessments for human safety
(e) 聽In conjunction with the regulatory team (project manager, residue experts, etc.) reflect on the 聽overall human safety of the agrochemical products in their intended use
(f) Communication with third party consultants / CRO鈥檚 for management and monitoring of experimental studies