Label Coordinator & Technical Documentation Specialist

CATALYST NUTRACEUTICALS:is dedicated to manufacturing premium-quality dietary supplements that set the standard for excellence in the industry.

We take pride in every product we produce and are committed to delivering exceptional quality, value, and innovation.

Our success is built on strong partnerships with employees, customers, suppliers, and industry experts, allowing us to stay ahead of market trends while maintaining the highest standards of service, pricing, and product integrity.

At Catalyst Nutraceuticals, quality isn't just a goal, it's the foundation of everything we do.

Position Reports to: Technical Documentation and Product Regulatory Manager Position Summary: The Label Coordinator and Technical Documentation Specialist is responsible for reviewing and maintaining technical documentation and information pertaining to all products and ingredients, and for working directly with customers to review, revise, and approve label and packaging artwork.

This role acts as a liaison between Development, Quality, external customers, and vendors to produce compliant technical documentation and packaging within a rapidly evolving regulatory environment.

As a member of the product development team, this individual is critical to facilitating the Label Panel Review (LPR) processmanaging customer artwork submissions, communicating findings and observations, and maintaining the latest approved artwork revisions and files.

This individual will understand and apply regulatory concepts through technical information and regulatory references to substantiate product content claims for new and existing products, supporting customer compliance requests.

Essential job Duties/responsibilities: Manages the submission of Labels for customer sign-offs and subsequent internal communicationsResponsible for initiating label deviations and change controls as designated by matrix of responsibilityReview customer artwork and labels for complianceWork 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 approvalLog and track all customer artwork submissions in the Label Review Tracker and communicate LPR findings (mandatory changes required for FDA compliance) and observations (recommended improvements) back to the customer for revision or sign-offManage version control of label and packaging artwork, maintaining the most current approved digital files in the approved label folder and re-validating artwork (e.g., confirming files older than six months remain valid) prior to reorderCoordinate artwork revisions and label transitions (soft and hard changes) with customers, accounting, and the packaging quarantine/destruction process to ensure only approved artwork is used in productionCompare vendor printers proofs against the last approved digital file for content and size accuracy prior to production approvalCoordinat...