Regulatory Affairs Executive - Medical Devices
MACOM · Delhi · onsite · Posted 21d ago
Undisclosed1–3 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- 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.
Sourced from naukri
Skills
Regulatory Affairsregulatory submissionsDossier PreparationTechnical Documentationcompliance
About MACOM
MACOM
Internet
375
employees
1950
76 years old
Thrissur, Kerala
India
₹3.1L PA avg
Avg at MACOM
About
MACOM Technology Solutions focuses on general construction services, prioritizing quality refurbishment and client satisfaction in the building sector.
Industries
InternetManufacturingElectronics
Employee ratings
10 reviews
3.3/ 5
Culture
2.5
Career growth
2.1
Work-life
2.6
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