Nupur Tomar

Quality Assurance professional with 1 year 4 months of experience in pharmaceutical manufacturing, with hands-on experience in QMS, documentation control, GMP compliance, and quality systems management. Experienced in SOP management, BMR/BPR control, CAPA and deviation-related activities, audit support, and Data Integrity compliance. Adept at ensuring compliance with cGMP, GDP, ALCOA+, and regulatory requirements while supporting quality system activities.

Quality Assurance Officer - All Cure Pharma Pvt. Ltd. - Bahadurgarh, Haryana

(2023-12 - 2025-04)

• Prepared, reviewed, revised, issued, and controlled GMP documents including SOPs, BMRs, BPRs, specifications, formats, logbooks, and records.
• Managed document control activities, document issuance, archival, retrieval, reconciliation, and maintenance of master lists and registers.
• Assisted in handling Quality Management System (QMS) activities including Deviations, CAPA, Change Controls, and training compliance tracking.
• Reviewed manufacturing, packaging, and departmental records/logbooks to ensure compliance with cGMP, GDP, and ALCOA+ Data Integrity principles.
• Coordinated with Production, QC, Warehouse, Engineering, and other departments for documentation compliance and timely closure of quality events.
• Maintained SOP training records, document registers, and item code databases.
• Supported internal audits, self-inspections, regulatory audit readiness, investigation activities, root cause analysis, and CAPA effectiveness verification.
• Ensured effective implementation and continuous improvement of Quality Management Systems in accordance with regulatory and company requirements.

Master of Science (M.Sc.) - Microbiology - CCSU (2022)

Bachelor of Science (B.Sc.) - CCSU (2019)