Jr. Regulatory Affairs Executive
Published date: 2026/11/06
- Location: Ahmedabad, Gujarat, India
Knowledge of ISO 9001, ISO 13485, CE, US-FDA (510K), Other Regulatory & CDSCO Guidelines.
Planning, review and submission of Documents as per Country Specific regulatory guideline in medical device registration.
Prepare and maintain technical file and medical device master files as necessary to obtain and sustain product approval.
Keeping records to documents and samples of different Countries.
Co-Ordination with respective
Planning, review and submission of Documents as per Country Specific regulatory guideline in medical device registration.
Prepare and maintain technical file and medical device master files as necessary to obtain and sustain product approval.
Keeping records to documents and samples of different Countries.
Co-Ordination with respective
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