Lead, Regulatory Specialist

Voyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve.

Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated.

We invest in their growth, providing opportunities for development and advancement within our dynamic team.

Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products.

We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs.

This can include skincare, haircare, bath and body products, fragrances, and more.

Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.

Safety is a core value at Voyant Beauty.

We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.

If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you.

Come join us and be a part of our journey.

A Brief Overview

The R&D Lead Regulatory Specialist is responsible for ensuring cosmetic and OTC formulations, raw materials, and finished products comply with all applicable regulatory requirements throughout the product development lifecycle.

This role partners closely with R&D, Quality, Supply Chain, Manufacturing, Marketing, and Legal to interpret regulations, assess compliance risk, support product innovation, and maintain regulatory documentation for domestic and global cosmetic markets.

The position serves as a regulatory subject matter expert and key business partner, balancing innovation speed with compliance integrity while supporting both internal teams and contract manufacturing clients.

What you will do


* Evaluate cosmetic and OTC formulations, raw materials, and packaging for compliance with applicable regulations (FDA/MoCRA, 21 CFR 210/211, Prop 65, EU 1223/2009, Canada, Japan, and other major markets as required).


* Review ingredient usage levels, labeling, claims, and product positioning to ensure regulatory compliance and substantiation alignment.


* Partner with R&D during concept development, reformulations, and scale-up activities to provide regulatory guidance and risk assessment.


* Support regulatory submissions and product notifications (e.g., FDA listings, CPNP, regional systems) and maintain Product Information Files (PIFs).


* Review and assess supplier documentation including specifications, SDS, allergen disclosures, regulatory statements, and certifications.


* Monitor global regulatory changes and conduct regulatory impact assessments on existing and new formulas.


* Maintain regulatory documentation within internal systems and ensure data accuracy and audit readiness.
...