Regulatory Affairs Associate

• Reviewing ingredients for regulatory compliance for different markets and product categories. 
• Partner with manufacturers and ingredient suppliers to acquire all necessary documentation to maintain an accurate library of robust products and raw materials. 
• Prepare, compile, and organize all relevant documentation for product registrations and listings. 
• Ensure renewals for state licenses. 
• Maintain business systems, databases, and knowledge sharing systems as appropriate.   
• Coordinate FDA Drug Listing submissions for Rx and OTC products under supervision from Regulatory Leadership 
• Ensure appropriate follow-up correspondence, such as re-submissions, re-certifications, renewals as required. 
• Other duties as assigned by the Supervisor. 

• A bachelor’s degree from an accredited university is required. A focus in Life Sciences or Chemistry is highly preferred. 
• At least 3-4+ years of relevant experience within regulatory affairs; familiarity with regulatory frameworks across various jurisdictions and a keen ability to accurately interpret and apply them real time. 
• Exceptional organizational and prioritization/time management skills; demonstrated ability to work under pressure to meet deadlines. 
• Comfortable operating in a fast paced, ever-changing environment; someone who thrives in ambiguity and adapts quickly.  
• Proficiency in Microsoft Office and other technologies. 
• An energetic, positive attitude that encourages a team and supports the growth and professional development of others. 

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