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Job Location | Delhi |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | ales / BD |
EmploymentType | Full-time |
1. RA team handling2. Dossiers / Documents review3. Guidelines of different regulatory authority updation to team.4. Arranging documents from plant5. Liasioning with plant QA / QC / Production.6. Artwork text approval.7. FSC / COPP new and renewal of all products8. Dossier monthly planning and achievement9. Handling of NOD and timely reply10. Plant visit for proper Liasioning.
Keyskills :
assurancequalitypharmaceuticalsregulatoryofficeaffairs