This is a work-from-home position

Snowberry.kr is seeking an experienced Regulatory Affairs & Compliance Chemist with robust hands-on knowledge of cosmetic formulation, manufacturing, product documentation, labeling and international cosmetic regulations that covers US / Canada / EU / UK.

This is not simply a filing or paperwork position. The successful candidate must understand how cosmetics are actually formulated and manufactured, be able to identify missing or weak technical documentation, and have the confidence to stop non-compliant products or practices from proceeding.

Key Responsibilities
Review cosmetic formulas for compliance in the USA, Canada, European Union and United Kingdom
Review ingredients, concentrations, restrictions, prohibitions and conditions of use
Maintain complete regulatory files and supporting technical documentation for every product
Identify missing documentation and actively obtain or create the required records before product release
Review product labels, INCI declarations, warnings, directions, claims and mandatory statements
Verify that marketing and product claims are properly supported
Review formula changes,



ingredient substitutions and manufacturing changes before implementation
Ensure approved formulas and specifications match what is actually manufactured
Review manufacturing records, specifications, certificates and supporting supplier documentation
Support or maintain required market notifications, registrations and product files
Maintain accurate version control and regulatory approval records
Investigate regulatory gaps, deviations and historical compliance issues
Develop corrective actions where existing products or processes do not meet requirements
Keep the company current with regulatory changes in all four markets

Success in This Role
No product proceeds to market with unresolved regulatory deficiencies
Complete and current regulatory files for every active product
Formula, label and manufacturing records remain aligned
Regulatory changes are identified before they become business problems
Missing historical documentation is systematically corrected
All approvals are supported by evidence and clearly documented

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