We are seeking dedicated, full-time Scientific and Regulatory Toxicologist to join our expert team. Successful candidates should have experience with FDA and FTC regulatory compliance, toxicology, and experience with GRAS submissions, able to work remotely within a collaborative culture.

AIBMR Life Sciences, Inc. is a premier scientific and regulatory consulting firm specializing in GRAS determinations, FDA and FTC compliance, toxicological safety assessments, and publication of peer-reviewed safety assessments. For over 45 years, we have provided clients worldwide expert regulatory guidance and/or assessments of novel ingredients and food products introduced into the U.S. market.

Key Responsibilities:

• Manage assigned projects involving GRAS self-determinations (Independent Conclusions of GRAS Status), GRAS Notifications to FDA, and New Dietary Ingredient (NDI) Notifications.
• Interpret toxicology studies (acute, subchronic, developmental, genotoxicity, etc.).
• Prepare and critically review toxicological safety assessments for food ingredients, dietary supplements, pet foods, and cosmetics.
• Co-author scientific manuscripts for peer-reviewed publication in support of regulatory dossiers from a toxicological viewpoint.
• Ability to contribute to scientific and strategic problem-solving solutions.
• Remain updated on global regulations and scientific trends relevant to ingredient safety and compliance, and safety assessment technologies.

• Ph.D., D.Sc., N.D., DABT, or equivalent advanced degree in toxicology, medicine, food science, or related fields.
• At least 2 years of experience in scientific regulatory consulting, with a strong focus on FDA-regulated ingredients and food products.
• Experience with GRAS submissions to FDA, a plus.
• Ability to coordinate with expert panels.
• Track record in overseeing toxicological studies and their data interpretation.
• Publication record that demonstrates excellent writing skills.
• Excellent communication skills.
• Experience with global regulatory authorities (e.g., EFSA, Health Canada, etc.) a plus.
• Experience interacting with FDA or FTC on regulatory matters.
• Ability to work with a collaborative team.