Scientific Expert in Ecotoxicology

vor 1 Woche

Berlin, Deutschland Staphyt Vollzeit

**About us**:
We strengthen science together

Present in Europe, North Africa, South America, STAPHYT brings together more than 700 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.

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, REACH sectors. Skills, experience and geographical coverage are three essential assets of our team to enable our clients to achieve their regulatory affairs objectives.

**Mission**:
We are currently looking for an enthusiastic and motivated expert to join our multinational and expanding Environment Team in Europe. Ideally, you have a strong background in environmental risk assessments and study monitoring.

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.

**Main duties**:

- 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 relevant sections 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

**Profile**:
**Skills and experience required**:
**Essential**
- Relevant scientific degree
- At least 5 years experience in one or several relevant EU/UK regulatory regime(s), either gained as consultant, evaluator or within industry
- Ability to understand and accurately interpret data from studies and complex risk assessments 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
- Experience in monitoring/evaluation of laboratory tests and higher tier studies
- Ability to work independently
- Have a good attention to detail
- Be a good communicator
- A high level of written and spoken English

**Desirable**
- Knowledge of IUCLID

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