Manager, Global Regulatory Compliance

Job Description

Job Description

Core Duties and Responsibilities:

• Lead global regulatory strategy for product launches, reformulations, claims, and market expansion initiatives.
• Serve as the central point of coordination between U.S. regulatory requirements and international market execution.
• Maintain visibility over global registrations, renewals, submissions, and market-specific requirements.
• Identify and resolve regulatory risks before they impact launch timelines or business objectives.
• Monitor regulatory developments and translate changes into actionable business guidance.

• Partner with Product Development to evaluate ingredients, formulations, and claims early in development.
• Collaborate with Marketing to ensure claims and promotional materials are compliant and substantiated.
• Act as a trusted advisor to Product Development, Purchasing, Quality, and Customer Support teams.
• Drive communication across functions to improve speed-to-market and eliminate regulatory bottlenecks.

• Oversee regulatory submissions, certifications, registrations, and notifications.
• Review and approve labels, claims, promotional materials, and compliance-sensitive content.
• Ensure compliance with Health Canada, European Union, and other applicable international regulations.
• Manage relationships with external consultants and regulatory partners supporting global market access.
• Provide leadership, coaching, and development for direct reports.
• Serve as an escalation point and technical resource for complex regulatory issues.
• Foster a collaborative, solutions-oriented regulatory culture.

• Up to 25% travel with limited local driving required at times.
• 2 onsite days per week is an essential function of this position.
• Additional duties as assigned.

Position Requirements:

• Bachelor's degree in Regulatory Affairs, Life Sciences, Nutrition, Food Science, or related field.
• 5+ years of regulatory compliance experience in dietary supplements or similar regulated industry.
• Advanced knowledge of FDA, DSHEA, cGMP, Health Canada, EU, and global market-entry requirements.
• Experience supporting international product registrations and commercialization activities.

• Strong communication, project management, analytical, and stakeholder management skills.

• Ability to influence cross-functional teams and translate regulations into practical business solutions.
• Proficiency with Microsoft Office applications.