Associate Manager, Regulatory & Scientific Affairs

About this role

Responsibilities

• Provide regulatory oversight and guidance for dietary supplements, food ingredients, and natural health products in the US and Canada.
• Prepare, review, and submit regulatory dossiers and filings, including GRAS notices, NDINs, PLA, Master Files, and CMC documentation.
• Support the development and execution of regulatory strategies for Health Sciences in collaboration with the Global Regulatory Business Partner.
• Serve as the Regulatory Lead on cross-functional projects, ensuring regulatory considerations are embedded throughout development and commercialization.
• Provide regulatory guidance to Quality teams related to GMP compliance, product labeling, and associated regulatory requirements.