Food and Regulatory Toxicologist

Qualityhub; United States; Remote; USD 70,000 - 110,000; Full time

Job summary

A leading consulting firm seeks a Food and Regulatory Toxicologist to join its team. The ideal candidate will hold an advanced degree and have significant experience in FDA regulatory compliance, especially in GRAS submissions. This remote position emphasizes collaboration and mentorship, contributing to critical safety assessments for food ingredients and dietary supplements.

Qualifications

• Ph.D., D.Sc., N.D., DABT, or equivalent advanced degree in toxicology required.
• At least 2 years of experience in scientific regulatory consulting needed.
• Strong focus on FDA-regulated ingredients and experience with GRAS submissions is essential.

Responsibilities

• Manage client projects for GRAS status and FDA notifications.
• Design and interpret toxicology studies across various types.
• Prepare and review toxicological safety assessments.

Skills

Excellent communication skills

Scientific and strategic problem-solving

Toxicology study oversight

Education

Ph.D., D.Sc., N.D., DABT, or equivalent advanced degree in toxicology

Advanced degree in pharmacology, medicine, food science, or related fields

Job description

Food and Regulatory Toxicologist

AIBMR Life Sciences, Inc.

Location: Remote (U.S.-based candidates preferred). Headquarters: Seattle; Information Services Center, Oro Valley, AZ.

Job Type: Full-time

About Us:

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.

Position Summary:

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 with a collaborative.

Key Responsibilities:

• Assigned client projects involving GRAS self-determinations (Independent Conclusions of GRAS Status), GRAS Notifications to FDA, and New Dietary Ingredient (NDI) Notifications.
• Design, monitor, and interpret toxicology studies (acute, subchronic, developmental, genotoxicity, etc.).
• Prepare and critically review toxicological safety assessments for food ingredients, dietary supplements, 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.
• Provide mentorship and technical leadership to colleagues.
• Remain updated on global regulations and scientific trends relevant to ingredient safety and compliance, and safety assessment technologies.
  

Qualifications:

• Ph.D., D.Sc., N.D., DABT, or equivalent advanced degree in toxicology, pharmacology, medicine, food science, or related fields.
• At least 2 years of experience in scientific regulatory consulting, with a strong focus on FDA-regulated ingredients.
• Experience with GRAS submissions to FDA.
• Ability to coordinate with expert panels.introduced into
• 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.

How to Apply:

Please email your cover letter, CV, and publication history, and relevant project experience to:
[e-mail]

Applications will be reviewed on an ongoing basis until the positions are filled.