Human Health Risk Assessor

vor 1 Woche

Genève, Schweiz FMC Corporation Vollzeit

**Human Health - Risk Assessor**:
**Geneva (Hybrid)**:
**About us**

We, FMC Agricultural Solutions, provide innovative crop protection solutions to growers around the world. Thanks to the commitment of our over 5,000 employees, we are one of the six largest crop protection manufacturers in the world.

For our Geneva site we are looking for a **Human Health Risk Assessor.**
- This role reports to the FMC Corporation’s Global Regulatory Sciences group and is part of the Global R&D organization.
- As a competency expert in human health risk assessment, your role will be focused on developing the scientific data needed for new and existing molecules to help farmers maintain a safe and secure food supply, while protecting the public health and the environment for future generations.
- The position is office-based (hybrid) and located in our Geneva premises, responsibilities include regulatory work that supports our global business, with opportunities to interface with people around the world.
- The Global Regulatory Sciences group offers a unique balance of individual responsibilities and a team-focused project approach, providing our scientists with opportunities to engage in proprietary molecule development, learn regulations around the world, and invest in their professional development.
- Serves on Product Registration Team (PRT) as lead for asset
- Sets scientific strategy for projects relevant to asset, interfaces across disciplines
- Communicates science in submission packages, positions data within the context of regional/country registrations, responds to regulatory authority questions
- Technical program designer for projects.

**Key Responsibilities**
- You will work across an interdisciplinary sciences team as the competency lead in human health risk assessment.
- You will have responsibility for setting strategy for the technical program and collaborating with competency scientists and other team members to deliver the demands of the technical program.
- You will be responsible for developing data in support of our assets to meet the regulatory requirements of countries.

**Qualifications**
- Ph.D. in Pharmacology, Toxicology, Risk Assessment Modeling or closely related discipline, such as metabolism or residue chemistry. 5 years of relevant work experience in a commercial setting.
- Complete understanding of occupational exposure studies including mixer/loader/applicator and worker re-entry, dermal penetration studies, and non-dietary exposure studies.
- Communicates research directions within the R&D community.
- Effectively communicates how individual research efforts are integrated into those of the overall team.
- Seeks increased personal responsibility and takes responsibility for others to drive organizational or research goals.
- Adjusts communication and interpersonal approach depending upon the audience, constructive critical debate and decision making. Reviews and reports group efforts.
- Can communicate effectively in both technical and non-technical situations and across all levels. Actively initiates effective information exchanges.
- Promotes and uses anticipatory problem-solving techniques to address issues before they become problems.
- Effectively manage numerous tasks/projects simultaneously to meet internal/external deadlines while maintaining organizational integration within a global scientific support team.
- Ability to design and manage appropriate field and analytical studies under FIFRA, OCSPP and OECD guidelines.

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