Aseelah Harrison

At Zoetis, I support CQV and method verification while testing injectable canine medications and creating SOPs, transfer methods, and OJTs for QC chemistry instrumentation.

Previously at Amgen, I performed method validation and transfer across chromatography, bioassay, PCR, microbiology, immunoassay, capillary electrophoresis, gel, device, viral, and compendial methods. I created validation reports and appendices while critically analyzing analytical data in a fast-paced, multidisciplinary environment.

My quality background also includes release testing and investigations at Dendreon Pharmaceuticals, microbial QC and regulatory submission support at Intralytix, and quality engineering for nanocrystal products at Pixelligent Technologies. I’ve led analysts, optimized laboratory processes, applied 5 WHYS root-cause analysis, and written SOPs, protocols, specifications, and quality documents.

I hold an M.S. in Biochemistry and a B.S. in Chemistry, with hands-on experience across chemistry, biochemistry, biotechnology, nanotechnology, cGMP, and GLP environments.