
Executive
4 days ago
**Title**:EXECUTIVE**:
- Date: Sep 3, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**Position**: Exe / Sr. Exe (Regulatory Affairs, Baroda)
**Grade **- G12A/G11B
**Education** - B.Pharm / M. Pharm
**Experience** - 4 to 6 years
**Location** - R&D - Baroda
- Review all data and documents related to product registrations for various health authorities.
- Compile registration dossiers for submission to various health authorities like - US-FDA, Health Canada, Europe, Australia/New Zealand, Japan and Israel.
- Prepare responses to deficiency letters received from various agencies.
- Maintain life-cycle / post approval changes for drug product registration dossiers.
- Provide regulatory support to cross functional departments.
- Prepare and submit scientific advice to various health authorities.
- eCTD compilation, verification and submission through electronic gateway
- Review, preparation and submission of annual reports to US FDA
- Review, preparation and submission of post approval supplements to US FDA
**Position**: Exe / Sr. Exe (Regulatory Affairs, Baroda)
**Grade **- G12A/G11B
**Education** - B.Pharm / M. Pharm
**Experience** - 4 to 6 years
**Location** - R&D - Baroda
- Review all data and documents related to product registrations for various health authorities.
- Compile registration dossiers for submission to various health authorities like - US-FDA, Health Canada, Europe, Australia/New Zealand, Japan and Israel.
- Prepare responses to deficiency letters received from various agencies.
- Maintain life-cycle / post approval changes for drug product registration dossiers.
- Provide regulatory support to cross functional departments.
- Prepare and submit scientific advice to various health authorities.
- eCTD compilation, verification and submission through electronic gateway
- Review, preparation and submission of annual reports to US FDA
- Review, preparation and submission of post approval supplements to US FDA
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Executive
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Executive
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Executive
3 days ago
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