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.