We are seeking a highly organized and detail-oriented M.Pharma qualified to support documentation, record management, and regulatory compliance activities for our medical device manufacturing operations. [email protected] or (phone hidden)
Required Candidate profile
Strong 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
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