Job highlights
4+ years experience in Medical Device Regulatory Affairs with expertise in CDSCO & EU MDR submissions
Handle regulatory submissions, prepare technical documentation, and manage manufacturing licenses
Regulatory Affairs Executive/Assistant Manager - Medical Devices
4+ years of experience in Medical Device Regulatory Affairs.
Handle CDSCO & EU MDR (2017/745) regulatory submissions.
Prepare and maintain Technical Documentation, DMF, GSPR & CER.
Manage CDSCO manufacturing licenses, FSC, Test/Loan Licenses and related applications.