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Position Overview: As a Senior Mammalian Toxicologist, you will focus on developing research for new and existing molecules. You will serve as the competency expert on cross-functional teams and act as Study Monitor for a broad array of toxicology studies for EPA, EU, and other global regulatory agencies. This includes protocol preparation, interaction with contract scientists, and critical evaluation of data to provide final reports. You will collaborate with toxicologists, metabolism, human health risk assessors, and residue chemists to develop strategies addressing technical requirements through study design, new technologies, and best practices.
Responsibilities:
- Serve as the competency expert on cross-functional teams.
- Act as Study Monitor for various toxicology studies for EPA, EU, and other global regulatory agencies.
- Prepare protocols, interact with contract scientists, and critically evaluate data to provide final reports.
- Collaborate with toxicologists, metabolism, human health risk assessors, and residue chemists.
- Develop strategies to address technical requirements through study design, new technologies, and best practices.
Qualifications and Education:
- Ph.D. in Mammalian Toxicology, Pharmacology, or a closely related discipline with a publication record and 5-10 years of relevant work experience in a commercial setting. Or,
- M.S. in Mammalian Toxicology, Pharmacology, or a closely related discipline with 10-15 years of relevant experience.
- Broad scientific knowledge in mammalian toxicology, physiology, and/or veterinary medicine.
- Knowledge of toxicology studies (design and data generated) required for regulatory agencies.
- Experience interacting with regulatory agencies in the US, Europe, or globally through white papers or in-person meetings.
- Excellent oral and written communication skills, including scientific reports, hazard evaluations, and position papers.
- Knowledge of global regulation and GLP requirements for human health.
Additional Relevant Experience:
- Ability to manage multiple tasks/projects simultaneously to meet deadlines.
- Experience designing and managing toxicology studies under FIFRA, OCSPP, and OECD guidelines.
- Understanding of and experience with external industry working groups and regulatory initiatives.
Why FMC Corporation? The Global Regulatory Sciences group offers a unique balance of individual responsibilities and a team-focused project approach. This provides our scientists with opportunities to engage in proprietary molecule development, learn global regulations, and invest in their professional development.
EEO Statement
- At FMC, diversity and inclusion are in our DNA. We are proud to be an Equal Opportunity Employer with a commitment to creating an inclusive workplace where all employees can thrive – regardless of race, gender, sex, pregnancy, gender identity and/or expression, sexual orientation, national origin or ancestry, citizenship status, color, age, religion or religious creed, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, or any other basis protected by federal, state or local law. FMC also supports employee participation in company employee resource groups that celebrate the diverse backgrounds of our workforce by providing communities for employees to connect with each other and raise awareness throughout FMC.
- FMC complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities.
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