Coordinate with outside graphic artist and Sales/Marketing team to create and proofread all labeling for new and existing products.

Develop and proofread structured product labeling (SPL) files for OTC and Rx products.

Maintain the labeling for all marketed products in accordance with RLD and/or OTC monograph updates.

Compile all labeling needed for Regulatory submissions (i.e. new ANDAs, annual reports, supplements, and/or amendments)

Review and approve all labeling printer proofs, obtaining customer approval, if required.

Review and verify labeling components staged for packaging work orders.

Maintain the company’s Art Tracker database and all labeling files within the QA Labeling Department.

Participate in team meetings surrounding labeling issues.

Support other departmental personnel when needed.

2+ years pharmaceutical experience in a related position.  Bachelor’s degree preferred.

Strong knowledge of OTC monographs a plus.

Proficiency in Microsoft Office and Acrobat Professional required.

Excellent organizational skills with a strong attention to detail.

Excellent communication skills required to work interdepartmentally at every level, along with a clear focus on customer service.

Ability to work independently with minimal supervision in a fast paced, deadline driven environment.