Raw material compliance consultant supporting ingredient reviews and regulatory dossiers for ClinChoice, a global CRO. Assessing cosmetic compliance across FDA, EU, Health Canada, and ASEAN regulations.
Responsibilities
Support maintenance and updating of ingredient and raw material regulatory information in internal systems
Maintain regulatory compliance of raw material dossiers by reviewing data, performing gap analyses, and communicating with suppliers
Assess the impact of regulatory changes on the product portfolio under global cosmetic regulations, including FDA, EU, Health Canada, and ASEAN requirements
Review raw material documentation such as SDS, TDS, specification sheets, allergen statements, and regulatory declarations
Evaluate raw materials for restricted substances, labelling requirements, and safety concerns
Maintain and update internal databases and records
Collaborate with R&D, Regulatory, Quality, and Purchasing teams to resolve discrepancies
Assist with regulatory dossiers for product registration and claims substantiation
Requirements
Bachelor’s degree in Chemistry or a closely related scientific field (required)
Minimum of 2 years of experience in regulatory affairs, quality, or raw material review, preferably in cosmetics, personal care, or a related industry
Familiarity with global cosmetic regulations and ingredient restrictions
Excellent attention to detail and organizational skills
Excellent written communication
Proficiency in Microsoft Office (Excel, Word, Outlook)
Experience with regulatory databases is a plus
Excellent project management skills
Ability to manage multiple priorities and work in a fast-paced, collaborative environment
Benefits
Remote work option in Canada
Professional development and continuous training
Supportive culture
Equal opportunity and inclusive, barrier-free recruitment
Accommodation for qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act
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