Hybrid Analista Jr Master Data en Medline Industries, LP

Job Description

Main responsibilities:

Submission and review of component sourcing forms to suppliers.
• Confirmation/Review of information submitted to the FDA
• Confirmation/Review of withhold release list published by CBP
• Confirmation/Review of import alerts published by different government agencies
• Confirmation/Review of manufacturer registration numbers for components that require it.
• Confirmation/Review of Medical Device Listings (MDLs), 510K and COOs
• Confirmation, review and update of ingredients according to National Drug Code (NDC)
• Evaluate current components and identify potential issues related to Affirmation of Compliance Codes (AOC)
• Fill out component forms internally when applicable for the release of the same (AOC)
• Assignment and review of appropriate QW/CH codes for components
• Contact our suppliers when necessary to confirm information from FDA, CBP among others.
• Take photos of new components to upload them to our database (Munintra)

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.