Work Flexibility: Hybrid
- Basic understanding of the regulatory requirements under Medical Device Rules, 2017 and the Drugs & Cosmetics Act.
- Assist in preparing and organizing regulatory documentation and submissions for recent products and retentions.
- Support RA team in remediation activity for existing submissions / approvals
- Maintain and update regulatory databases, trackers, and filing systems.
- Conduct research on regulatory guidelines and updates issued by authorities.
- Track regulatory timelines and maintain submission status reports.
- Coordinate with internal teams to gather information required for regulatory

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- Support the Regulatory Affairs team with administrative and documentation tasks.
- Understand the complaint and adverse event reporting requirements and report such events to the competent authority within the stipulated timelines.

Understand the BIS registration process and requirements

Travel Percentage: 10%

📌 RAQA Intern (Gurugram)
🏢 Stryker
📍 Gurugram