Ensures compliance with MDR 2017 and global regulations.
Manages CDSCO submissions, authority liaison, and core technical docs.
Tracks regulatory updates; works with QA/R&D; to enable protected market access for SaMD & implants.
Required Candidate profile
B.Pharm/M.Pharm with 5+ years of experience in Pharma.
Solid understanding of medical device regulations (India, EU, US).
Knowledge of Medical Device Software (SaMD) regulations is a plus.
📌 Manager Regulatory Affairs Leading Pharma Mnc Kolkata (India)
🏢 Hindco Recruitment Consultants
📍 India
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