Posted:2 weeks ago|
Platform:
Work from Office
Full Time
To lead Regulatory affairs team engaged in dossier preparation in CTD and ACTD formats.
Responsible for final review of dossier before submission.
Reviewing artwork for products as per relevant regulatory authority requirements.
Coordination with F&D, QA, QC & Store for documentation
In-depth knowledge of pharmaceutical documentation & regulatory guidelines.
To coordinate with technical team for documents required for dossier.
Country Experience Preferred: CIS, LATAM
Dosage Form Experience: Soild Oral + Injectable
Opes Healthcare
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