Regulatory Affairs (RA) Associate

Job Overview

Cipla is looking for Regulatory Affairs executives to compile and submit dossiers for US, EU, and emerging markets.

Core Responsibilities

• Compile and review CMC data for eCTD submissions.
• Address queries from regulatory agencies (FDA, EMA) within timelines.
• Track regulatory updates and coordinate with production teams for compliance data.

Key Requirements & Skills

• M.Pharm or M.Sc. in Life Sciences.
• 2+ years experience in global dossier submissions.
• Detail-oriented with strong documentation skills.

Compensation & Benefits

• •Hybrid working flexibility.
• •Excellent corporate health benefits.
• •Annual performance bonuses.

How to Apply

Please send your resume/application directly to the recruiter's email: ifactselugu@gmail.com?subject=Application for RA Associate.