- 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
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