CA

AGM Regulatory Affairs - DGCI

Cadila Pharmaceuticals
Dholpur4-8 LPA Posted 11 Sept 2025
FULL TIME
Clinical Trials
Risk Assessment
Compliance Management

Job Description

Role & responsibilities

  • Liaison with Food & Drugs Control Administration, Gandhinagar/circle offices/CDSCO for various applications including but not limited to Product Permissions for manufacturing COPPs Various certificates for tender (FSC, Performance certificate, Non-conviction certificate) Inspections for WHO GMP/Schedule M GMP certification Technical persons approval Technical person application verification. Liaison with CDSCO, West Zone, Form 29 Export licenses Loan license Manufacturing licence renewal for all plants Wholesale licences Submission of commercial batches to CDL Kasauli for testing Submission of quarterly returns to NCB/CBN Handling NSQs Experience in submissions through Sugam, NSWS and ONDLS portals
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