Regulatory Affairs Executive
2 weeks ago
Job Description:
- CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards.
- Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market.
- Review of technical documents before filing on CDSCO portal.
- Proper knowledge of Medical Device Rules 2017 and other ISO standards for medical device.
- Well aware with BIS registration, ISI/FMCS registration, BEE registration, WPC approval, FDA registration, Legal Metrology registration, Pollution NOC and Waste management compliance.
- Must know to handle/manage technical queries related to CDSCO (MD, Drug & Cosmetic) registration for client.
- Working experience in documentation required for quality certification.
- Knowledge of quality certification (ISI mark) of different products as per BIS norms
- Working experience in designing various testing machines as per Indian standards.
**Salary**: ₹15,000.00 - ₹35,000.00 per month
**Benefits**:
- Cell phone reimbursement
Schedule:
- Day shift
Work Location: In person
**Speak with the employer**
+91 9311440661
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