We are seeking a highly organized and detail-oriented M.Pharma professional to support documentation, record management, and regulatory compliance activities for our medical device manufacturing operations.
[email protected] or (phone hidden)
Required Candidate profile
Solid understanding of documentation control and record management.
- Knowledge of ISO 13485, Medical Device Rules (India), CDSCO regulations, and Good Documentation Practices.
📌 Documentation & Regulatory Affairs Executive-Diary circle-Bangalore (Bengaluru)
🏢 Brains N Skills Chennai
📍 Bengaluru