Junior Toxicologist - Erlanger, KY
Archer Daniels Midland
Junior Toxicologist - Onsite in Erlanger, KY, Decatur, IL, Chicago, IL, OR Cranbury, NJ
Position Description:
This position is to provide Toxicology and Product Risk Assessment support to the Regulatory and Scientific Affairs groups, and in support of Quality and Food Safety, or as needed to other DM units for all areas of the company. Principal activities are:Generate and/or compile literature, in-silico, in-vitro and/or in-vivo safety data supporting regulatory documentation, registration dossiers, GRAS assessments, and risk assessments for ADM products and R&D projects across the enterprise portfolio that includes flavors, colors, food and beverage ingredients, dietary supplements, biotics, for humans and animals. Activities will also support cosmetics, pharma, and other industrial use opportunities as needed.Ability to review, navigate, and advise globally on competent authority requirements and scientific and industry positions that impact ADM. Providing safety (tolerance), efficacy, and other scientific assessments.Monitor and evaluate scientific literature to support day-to-day business activities to support product safety, new product development, expansion and maintenance of current product use.Provide timely communication of regulatory and scientific events, and timely progress reports to RSA leadership, as well as relevant units within ADM.Demonstrates good information and knowledge management practices, organization, project management and portfolio support, maintain databases and supportive documentation and participate as an active member of the regulatory science community.Demonstrates ability to expand application of knowledge and experience to new categories with appropriate support and exposure and work independently on projects related to these new categories of expertise.Requirements: Ph.D. degree in Chemistry, Biochemistry, Physiology, Pharmacology, and/or Toxicology. Toxicology coursework or emphasis required Toxicology research or work experience requiredSome industry toxicology experience desired but not required.Commitment to obtain DABT certification within 3-5 yrs of full-time employment.Strong critical thinking, excellent writing and communication skills are requiredAbility to plan and execute multiple projects utilizing a variety of resources.Ability to lead through ambiguity, take initiative, strong and demonstrated data management and project management skills.Open mindset for learning and applying skills and knowledge to any product category.Excited about this role but don’t think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.
ADM requires the successful completion of a background check.
REF:103925BR
Position Description:
This position is to provide Toxicology and Product Risk Assessment support to the Regulatory and Scientific Affairs groups, and in support of Quality and Food Safety, or as needed to other DM units for all areas of the company. Principal activities are:Generate and/or compile literature, in-silico, in-vitro and/or in-vivo safety data supporting regulatory documentation, registration dossiers, GRAS assessments, and risk assessments for ADM products and R&D projects across the enterprise portfolio that includes flavors, colors, food and beverage ingredients, dietary supplements, biotics, for humans and animals. Activities will also support cosmetics, pharma, and other industrial use opportunities as needed.Ability to review, navigate, and advise globally on competent authority requirements and scientific and industry positions that impact ADM. Providing safety (tolerance), efficacy, and other scientific assessments.Monitor and evaluate scientific literature to support day-to-day business activities to support product safety, new product development, expansion and maintenance of current product use.Provide timely communication of regulatory and scientific events, and timely progress reports to RSA leadership, as well as relevant units within ADM.Demonstrates good information and knowledge management practices, organization, project management and portfolio support, maintain databases and supportive documentation and participate as an active member of the regulatory science community.Demonstrates ability to expand application of knowledge and experience to new categories with appropriate support and exposure and work independently on projects related to these new categories of expertise.Requirements: Ph.D. degree in Chemistry, Biochemistry, Physiology, Pharmacology, and/or Toxicology. Toxicology coursework or emphasis required Toxicology research or work experience requiredSome industry toxicology experience desired but not required.Commitment to obtain DABT certification within 3-5 yrs of full-time employment.Strong critical thinking, excellent writing and communication skills are requiredAbility to plan and execute multiple projects utilizing a variety of resources.Ability to lead through ambiguity, take initiative, strong and demonstrated data management and project management skills.Open mindset for learning and applying skills and knowledge to any product category.Excited about this role but don’t think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.
ADM requires the successful completion of a background check.
REF:103925BR
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