Food and Regulatory Toxicologist

Radiology Partners Gulf Coast; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

AIBMR Life Sciences, Inc. is seeking a full-time Scientific and Regulatory Toxicologist with expertise in FDA and FTC compliance. This remote position involves responsibilities in regulatory consulting, toxicology study management, and preparation of safety assessments for food ingredients and dietary supplements. Ideal candidates will have a Ph.D. and at least two years of relevant experience, combined with excellent communication and writing skills.

Qualifications

• Ph.D. or equivalent in toxicology, pharmacology, medicine, or food science required.
• At least 2 years of experience in scientific regulatory consulting.
• Strong publication record and excellent communication skills.

Responsibilities

• Manage GRAS self-determinations and FDA notifications.
• Design and interpret toxicology studies.
• Co-author scientific manuscripts for regulatory submissions.

Skills

FDA regulatory compliance

Toxicology

Communication

Scientific writing

Education

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

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.