Shruti Suryawanshi

Promoted from Junior Data Analyst to Case Finalizer within one year through strong drug safety compliance performance. Managed end-to-end adverse event case processing in Argus Safety, including medical narrative review, QC checks, and on-time regulatory submission.

Delivered medication dispensing and patient counseling, and supported pharmacy operations including inventory management. Maintained compliance and collaborated with healthcare professionals to support community health.

Supported Quality Assurance activities including SOP and BMR/BPR documentation, deviation handling, and CAPA processes. Assisted with WHO-GMP and Schedule M compliance, internal audits, production coordination, and QA/QC data review.

Completed a research traineeship focused on organic synthesis and multi-step reactions, including chromatography, NMR, IR/UV–Vis, mass spectrometry, and optical characterization. Conducted GMP-related regulatory compliance and characterization experiments for photoremovable protecting groups.

Activities and societies: Medication dispensing, patient counseling, inventory management; regulatory compliance and collaboration with healthcare professionals.

Provided pharmaceutical care including medication dispensing, patient counseling, and inventory management while maintaining regulatory compliance.

Activities and societies: PCR, qPCR, RT-PCR, gel electrophoresis, CRISPR/Cas9, western blotting, ELISA, microscopy, QSAR modeling, molecular docking; synthetic scheme work with purification and structural verification.

Completed a Master’s program in Pharmaceutical Biotechnology with laboratory and research training across PCR/qPCR/RT-PCR, CRISPR/Cas9 gene editing, and protein/assay workflows. Applied QSAR and molecular docking using VLife and Schrödinger to support drug-discovery efforts.

Completed a Bachelor’s of Pharmacy, building foundational expertise in pharmaceutical care and dispensing practices during training experiences.

Activities and societies: SOP, BMR/BPR documentation, deviation & CAPA, WHO-GMP/Schedule M, internal audits, production coordination, QA/QC data review.

Completed Quality Assurance-focused pharmaceutical training, supporting SOP and documentation work, deviation & CAPA handling, and GMP/GDP compliance. Participated in internal audits, production coordination, and QA/QC-related pharmaceutical data review.

Completed a Kathak Visharad diploma in Kathak dance, strengthening concentration, coordination, teamwork, and creativity.