Quality Assurance and Regulatory Affairs
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Quality and Regulatory professional with 2 years of experience supporting GxP-compliant pharmaceutical and clinical operations through strong QA documentation, audit readiness, and compliance execution. Proficient in deviation management, CAPA, change control, batch record review (BMR/BPR), SOP development, and data integrity (ALCOA+) to ensure consistent quality outcomes. Knowledgeable in GCP, ICH guidelines, and 21 CFR Part 11 requirements, with hands-on exposure to internal audits and regulatory support activities.
Proficient in Veeva Vault QMS, TrackWise QMS, SAP, LIMS, and MS Office Suite.
Regulatory Affairs Intern - Biogen, USA - USA
(2026-01)
Quality Assurance Specialist - Fortis Healthcare, Gujarat, India - Gujarat, India
(2022-07 - 2023-12)
Quality Assurance Intern - Fortis Healthcare, Gujarat, India - Gujarat, India
(2022-01 - 2022-06)
Master of Science - Regulatory Affairs - Northeastern University, Boston, MA (2024-01 - 2025-12)
Bachelor of Pharmacy - Pharmacy - Gujarat Technological University, Gujarat, India (2019-07 - 2023-07)