Nancy Verma

Executive Microbiology

Genip • Full-time

Dec 2025 - Present • 9 mos

Strong hands-on experience in pharmaceutical QC Microbiology with extensive involvement in validation activities and GMP documentation. Experienced in planning and executing microbiology validations, preparing detailed validation protocols and reports, defining acceptance criteria, preparing validation worksheets, recording and evaluating results, performing calculations, investigating deviations, and preparing final validation conclusions. Worked on validations related to purified water systems, microbiological media and media shelf life, autoclave/sterilization processes, environmental monitoring, and microbiological testing. Experienced in Microbial Limit Testing (MLT), TAMC, TYMC, specified microorganism testing, water analysis, environmental monitoring, Growth Promotion Testing, media preparation, and microbiological laboratory activities. Skilled in developing and reviewing SOPs, validation protocols, validation reports, sampling plans, worksheets, and other GMP documents with a focus on clear, practical, accurate, and audit-ready documentation aligned with applicable IP, USP, and GMP requirements.

Executive Microbiologist

Afternic • Full-time

Apr 2024 - Apr 2025 • 1 yr

Handled routine QC microbiology activities including environmental monitoring, purified water testing, sterility testing, microbial limit testing, growth promotion testing, media preparation and validation, and autoclave-related activities. Prepared and reviewed SOPs, worksheets, protocols, reports, sampling plans, and other GMP documentation. Maintained accurate records and supported laboratory compliance and audit readiness.