M
MACOM
Regulatory Affairs Executive - Medical Devices
Skills
Compliance
1 month ago
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Important information
Contract type:
Permanent
Location:
Delhi, India
Work mode:
Onsite
Published on:
1 October 2026
What they need
- 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.
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