Headline

B.Pharmacy Gold Medalist | Clinical Research & Pharmacovigilance Aspirant | GCP | Clinical Trials | Open to CRO Opportunities| Data Management Aspirant | MDL & Validation | Published Research Patent Co-Inventor.

About

A Bachelor of Pharmacy graduate from Malla Reddy Vishwavidyapeeth, currently contributing as an Analyst at DIVIS LABORATORIES. Gained hands-on exposure to pharmaceutical method development, RP-HPLC, regulatory compliance, and mass spectroscopy, with a strong foundation in ICH and QbD guidelines. Collaborated on Pharmaceutical Development & Support Center (PDSC) projects, focusing on analytical method development, formulation support, and process optimization. At DIVIS LABORATORIES, worked alongside teams to support analytical and formulation projects, leveraging scientific principles to address real-world R&D challenges. Committed to applying regulatory and compliance expertise to contribute to the organization’s innovative pharmaceutical solutions. Dedicated to fostering collaboration and bringing a methodical, research-driven approach to advancing development processes.

Location

Greater Hyderabad Area

Work experience

Apprentice at DIVIS LABORATORIES, Sep 2025 - Feb 2026 · 6 mos, • Worked in a GMP-compliant environment, ensuring adherence to SOPs, data integrity, and regulatory compliance aligned with clinical research standards. • Maintained and reviewed structured documentation, including analytical records, validation reports, and compliance documents, ensuring traceability and audit readiness. • Supported documentation practices aligned with GCP principles, ensuring accuracy, completeness, and version control. • Tracked and maintained study-related data using Excel-based systems, ensuring accurate and timely updates across multiple records. • Contributed to inspection readiness activities by maintaining high-quality documentation and supporting compliance checks. • Coordinated with cross-functional teams to ensure accurate data flow and timely study deliverables. • Reviewed datasets to identify inconsistencies, ensuring data quality and integrity across records. • Supported quality assurance processes contributing to audit-ready documentation and regulatory compliance. • Supported maintenance and organization of study documentation aligned with TMF structure and regulatory requirements.

Analyst at DIVIS LABORATORIES, Sep 2025 - Feb 2026 · 6 mos, Method development, mass spectroscopy,

Research Analyst at DIVIS LABORATORIES, Sep 2025 - Jan 2026 · 5 mos, • Ensured compliance with GMP standards while maintaining high-quality documentation and data integrity. • Supported cross-functional teams to facilitate accurate data flow and timely study deliverables. • Contributed to inspection readiness by maintaining structured documentation aligned with regulatory requirements.

Student at Malla Reddy institute of pharmaceutical sciences, Sep 2025

Education

Bachelor of Pharmacy - BPharm, Pharmacy, Pharmaceutical Sciences, and Administration, Malla Reddy Vishwavidyapeeth