Senior Scientist - Regulatory
Date: Feb 19, 2026
Location: Melville, NY, US, 11747
Company: ELC Beauty LLC
Description
The Estée Lauder Companies is seeking a Senior Scientist, U.S. Regulatory Affairs to lead compliance strategy for our cosmetics and personal care portfolio. This is a high-visibility role that combines deep technical expertise with the opportunity to shape U.S. regulatory strategy for a global prestige company. The ideal candidate will bring hands-on experience with FDA, EPA, and state-level cosmetic regulations, in addition to leadership skills that aim to influence cross-functional teams.
Regulatory Compliance & Stewardship
- Ensure compliance with the FDA Modernization of Cosmetics Regulation Act (MoCRA) and OTC drug regulations.
- Oversee Safety Data Sheets (SDS) to ensure accuracy and accessibility across regulatory systems.
- Lead compliance efforts for:
- California Proposition 65 chemical disclosures.
- CARB (California Air Resources Board) VOC restrictions.
- Washington State’s lead ban in cosmetics.
- Lacey Act requirements for sourcing botanical ingredients.
- Consumer Product Safety Commission (CPSC) Poison Prevention Packaging Act (PPPA) and General Certificate of Conformity (GGC) documentation generation and tracking.
- Support product stewardship, including TSCA (Toxic Substances Control Act) reporting and EPA-related obligations.
- Manage regulatory aspects of Cosmetic Ingredient Review (CIR).
- Maintain regulatory files, compliance reports, and documentation to support audits and inspections
Leadership & Strategy
- Serve as the U.S. regulatory subject matter expert, influencing R&D, Supply Chain, and Sustainability teams.
- Provide strategic input into regulatory advocacy through engagement with industry groups such as Personal Care Products Council (PCPC).
- Monitor and interpret emerging U.S. regulatory trends, advising senior leadership on compliance and business impact.
- Lead internal training programs to raise awareness of evolving federal and state requirements.
Safety & Cosmetovigilance
- Ensure compliance with MoCRA adverse event reporting requirements.
- Assess and document U.S. consumer complaints (causality, seriousness, expectedness)
Qualifications
- Strong working knowledge of FDA, EPA, CARB, Prop 65, TSCA, and state-level cosmetic laws.
- Experience in CIR submissions and regulatory advocacy.
- Excellent organizational, communication, and leadership skills.
- Bachelor or Masters Degree in Chemistry, Biology, Toxicology, or related discipline
- 5+ years of U.S. regulatory experience in cosmetics, personal care or OTX
Nearest Major Market: Long Island
Nearest Secondary Market: New York CIty