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Responsible for handling renewal and filing of registration applications with the Food and Drug Administration.
Monitoring and maintaining a systematic file of product dossier, CPRs, and LTOs.
Create and regulate Standard Operating Procedures in compliance with FDA standards.
Attend seminars, trainings, and public hearings.
Entertain customer inquiries regarding regulation and product information.
Perform tasks as may be required by superiors.

","identifier":{"@type":"PropertyValue","name":"Diamond Laboratories Inc","value":"209857"},"datePosted":"22 February 2024","validThrough":"2025-09-13 17:03:20","employmentType"

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