Open to opportunities

Indrani Ghosh

@indranighosh

Message

I process pharmacovigilance and medical device safety cases with regulatory precision.

India

Message

What I'm looking for

I'm looking to continue building my career in pharmacovigilance and medical device safety while exploring data science opportunities for further career advancement.

At Wipro, I process medical device complaints and pharmacovigilance safety cases, ensuring submissions, intake, investigation, and closure align with regulatory and client guidelines.

I've handled ICSRs across solicited, unsolicited, E2B, combination-product, literature, vaccine, serious, non-serious, fatal, and invalid case scenarios. I write concise case narratives, code adverse events and medical history using MedDRA, code drugs using WHODD, and support case processing and quality review workflows.

My pharmacology background includes published research on spermidine as a therapeutic strategy in neurological disorders. I'm committed to continuous learning and exploring data science opportunities while delivering accurate, timely safety reporting.

Experience

Work history, roles, and key accomplishments

Medical Device Complaint Processing Investigator

Wipro Ltd.

Dec 2022 - Feb 2026 (3 years 2 months)

Handled submission of medical device complaints to a safety database, processed safety records, and managed complaint intake ensuring adherence to timelines. Assessed regulatory cases per health authority guidelines and identified process improvements.

Safety Database Management Regulatory Compliance Process Improvement Case Investigation SOPs Time Management

Pharmacovigilance Associate

Wipro Ltd.

Sep 2020 - Dec 2022 (2 years 3 months)

Performed pharmacovigilance activities including data entry of ICSRs, case processing, and quality review. Applied regulatory guidelines to determine valid case reports and wrote concise case narratives.

Pharmacovigilance ICSR Case Processing MedDRA Coding WHO DD Guidelines Quality Review Argus Trackwise