Label & Regulatory Documentation Specialist

Kids for the Future; Buford (GA); On-site; USD 52,000 - 76,000; Full time

Job summary

CATALYST NUTRACEUTICALS is seeking a Label Coordinator and Technical Documentation Specialist to review and maintain technical documentation and product labels, and to work directly with customers to review, revise, and approve label and packaging artwork.

This role serves as a liaison between Development, Quality, and external partners, supporting the Label Panel Review process, tracking submissions, and ensuring FDA-compliant content and accurate artwork across revisions.

Qualifications

• 4 year college/university degree or 1-3 years’ related work experience.
• Having both education and experience preferred.

Responsibilities

• Manages the submission of Labels for customer sign-offs and subsequent internal communications
• Responsible for initiating label deviations and change controls as designated by matrix of responsibility
• Review customer artwork and labels for compliance
• Work directly with customers as the primary point of contact throughout the label and packaging artwork review and approval process, facilitating the Label Panel Review (LPR) from artwork receipt through final approval
• Log and track all customer artwork submissions in the Label Review Tracker and communicate LPR findings and observations back to the customer for revision or sign-off
• Coordinate artwork revisions and label transitions with customers, accounting, and the packaging quarantine/destruction process
• Provide insights into ingredient documentation, finished product specifications, nutritional facts/supplement facts, product development, and FDA compliance regulations

Education

Bachelor's degree

Tools

ERP software

Job description

CATALYST NUTRACEUTICALS is seeking a Label Coordinator and Technical Documentation Specialist to review and maintain technical documentation and product labels, and to work directly with customers to review, revise, and approve label and packaging artwork.

This role serves as a liaison between Development, Quality, and external partners, supporting the Label Panel Review process, tracking submissions, and ensuring FDA-compliant content and accurate artwork across revisions.