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.

Pay: ₹20,000.00 - ₹35,000.00 per month

Advantages:
Cell phone reimbursement

Schedule:
Day shift

Work Location: In person

📌 Drug Regulatory Affairs Noida
🏢 Corpseed ITES
📍 Noida