At Eden Pharma, I established and organized microbiology laboratory workflows while monitoring sterile and non-sterile areas through viable counts and non-viable particle counts. I also conduct bioburden testing of raw materials and maintain laboratory logbooks, raw data inventories, and SOPs.
My current QA work includes line clearance, documentation control, batch and manufacturing records, and validation and qualification documentation. I support audits, CAPA management, change control, and deviation investigations within the QMS.
At Aulton Pharmaceuticals and Nutraceutical, I performed BET, microbial limit testing, antibiotic bioassays, and sterility testing of raw materials, in-process products, and finished products. I also investigated sterility test failures, drafted OOS/OOT reports, and assisted with deviation and CAPA risk assessments.
I started in pharmaceutical quality control as an internee at Welmark Pharmaceutical, assisting with media preparation, logbooks, and basic data entry under GDP guidelines. I hold a Bachelor of Science in Microbiology from the University of Haripur and have experience with cGMP/GLP compliance, regulatory documentation, and Microsoft Office.
