Manager Regulatory Affairs Leading Pharma Mnc Chennai

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 secure market access for SaMD & implants.

Required Candidate profile

B.Pharm/M.Pharm with 5+ years of experience in Pharma.

Robust understanding of medical device regulations (India, EU, US).

Knowledge of Medical Device Software (SaMD) regulations is a plus.