05 Oct
|
MACOM
|
New Delhi
Manage regulatory submissions, registrations and approvals for medical devices.
Prepare and maintain regulatory documentation, dossiers and technical files.
Ensure compliance with applicable medical device regulations and guidelines.
Coordinate with internal teams for regulatory documentation and product approvals.
Track regulatory submissions, renewals, licenses and changes.
Support product registration, amendments and regulatory audits.
📌 Regulatory Affairs Executive Medical Devices New Delhi
🏢 MACOM
📍 New Delhi