Drug Regulatory Affairs
17 hours ago
**Key Responsibilities**:
- Compile and submit dossiers (CTD/eCTD format) for product registration, renewals, and post-approval changes.
- Ensure products comply with national and international regulations (e.g., FDA, EMA, WHO, CDSCO).
- Maintain regulatory databases and product registration records.
- Communicate with health authorities and respond to queries and deficiencies.
- Stay updated with changing drug regulations and guidelines.
Pay: ₹218,393.29 - ₹1,063,874.78 per year
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Work Location: On the road
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