08 Sep
|
Polymed
|
New Delhi
1. Prepare, review, and maintain regulatory documentation (dossiers, registration files, certificates, product information, etc.)
2. Coordinate with sales & marketing team to collect required documents and information for product registrations and submissions. 3. Liaise with the factory regulatory department to ensure timely preparation and availability of technical files, test reports, and supporting documents.
3. Assist in submission of product registration, renewals, and regulatory approvals as per international requirements.
4. Maintain regulatory records, approvals, and databases for accuracy and completeness for each International customer/ market.
5. Support in responding to regulatory queries from international customers or distributors.
6. Ensure all documents follow company SOPs, regulatory guidelines, and quality system requirements.
7. Provide regular status updates of ongoing regulatory submissions to sales teams and management.
📌 Walk-in || Regulatory Affairs (New Delhi)
🏢 Polymed
📍 New Delhi