Mammalian Toxicologist

FMC Corporation is a Fortune 1000, diversified chemical company serving agricultural, industrial and consumer markets globally for more than a century with innovative solutions, applications and quality products. As a global leader utilizing advanced technologies and customer-focused research and development, FMC provides innovative and cost-effective solutions to food and agriculture, pharmaceutical, pulp and paper, textiles, glass and ceramics, rubber and plastics, lubricants, structural pest control, turf & ornamental markets, specialty and related industries. Based in FMC Corporation’s Princeton, NJ Research Center this key R&D role is available because of continued expansion of business focus in this area. In this key s position, you will be able to utilize your knowledge and experience, to further develop your career. This position is for a Mammalian Toxicologist to provide support of the registration of agrochemicals worldwide. The position requires knowledge of toxicology study types, experimental design, and data/results to meet global agency requirements. Responsibilities: • Works with team to provide insight on the toxicity of active ingredients or formulations technologies. • Design and oversee toxicology studies to address regulatory requirements in the U.S. under FIFA and other regulatory agencies . • Evaluates the toxicity of new formulations including literature review of toxicology information on inert ingredients, contracting testing where appropriate and interpreting results for formulation chemists. • Review new product MSDS to ensure accuracy of information and OSHA compliance. • Maintains databases of toxicology information on formulations and active ingredients. • Study monitor for contracted studies, including acute, sub-chronic, developmental toxicity and other special studies. This includes protocol preparation, test material transmittal, business agreements, working with quality assurance auditors and the study director to provide a final report. • Preparation of responses for regulatory authorities globally. • Provide scientific expertise through review and comment on internal documents and supporting materials as well as proposed and on-going projects. ,,X Prepare critical reviews, risk assessments, “white paper” advocacy documents, scientific rationales, position statements related to FMC products. ,,X Attend professional meetings and task forces of special interest to FMC businesses (primarily agricultural products related). Publish or present scientific information at meetings and in journals.

Job Requirements:
Experience: ,,X Basic understanding of design and endpoints for routine toxicity studies ,,X Experience with toxicology studies, methods and protocols. ,,X GLP study work with FIFRA products ,,X Knowledge and use of Risk Assessment Models ,,X Effective oral and written communication ,,X Computer literate, experience with Microsoft Office products Beneficial Experience ,,X Registration support for agrochemical or specialty chemicals ,,X Effective interaction with Regulatory agencies in the US and Europe ,,X Participation in scientific societies, associations, and task forces. Education: ,,X Grade 16: M.S. with 3-10 years experience in toxicology hazard assessment, data analysis, GLP study design and monitoring If you are talented and possess a drive to achieve, then consider further building your career with FMC. Employees enjoy very competitive compensation, a full menu of work/life benefits and opportunities to continue developing their skills and expanding their career. FMC is an Equal Opportunity Employer, EEO, AAE, MFDV and supports a drug free workplace.

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