Jolly Dhar
QA/RA specialist | Medical device reporting | Regulatory affairs | post market surveillance | New product development | Software Medical device | US FDA | ISO 13485 | ISO 14971 |
- Role
- Mdr Analyst at Genpact
- Location
- Gurugram, HR, IN
- LinkedIn followers
- 500 followers
About Jolly Dhar
Working at Genpact in the Medical Device Reporting role has been a highly enriching…
Experience
Mdr Analyst
May 2024 — Present · Gurugram, IN
As a Medical Device Reporting Analyst, I specialize in the collection, analysis, and reporting of adverse events, device failures, and other safety-related incidents involving medical devices. I ensure compliance with regulatory requirements, including FDA and global reporting standards, and work cross-functionally with quality assurance, regulatory affairs, and clinical teams. My role involves data analysis, risk assessment, and the preparation of detailed reports to ensure timely and accurate submission to regulatory bodies, thereby supporting patient safety and company compliance.
Education
Rungta College of Pharmaceutical Sciences Kohka-Kurud Road
Diploma in pharmacy
2015 — 2017
Rungta College of Pharmaceutical Sciences Kohka-Kurud Road
Bachelor's in pharmacy
2017 — 2020
Shri Shankaracharya Technical Campus
Masters in pharmacy
2020
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