
About Ego Pharmaceuticals
Founded in Melbourne, Australia in 1953, Ego Pharmaceuticals has grown from a small compounding laboratory into one of the country's most respected manufacturers of dermatological, skincare, and topical pharmaceutical products. The company's product portfolio is built on a foundation of trusted pharmaceutical-grade ingredients — glycerin, liquid paraffin, and petroleum jelly among them — that demand consistent, accurate, and regulatory-compliant analytical testing, day in and day out.
Behind that consistent quality sits a Quality Control (QC) laboratory that runs a broad and demanding spectrum of compendial tests: appearance, pH, density, viscosity, Karl Fischer water determination, UV/Vis assays, titration, Loss on Drying, HPLC, GC and more. For the analysts who work there, the pressure to maintain both throughput and data integrity to British Pharmacopoeia (BP), European Pharmacopoeia (EP), and United States Pharmacopeia (USP) standards is relentless.
Coordinating that work — and quietly driving a revolution in how it is done — is Ego’s Analytical Development Team. They first asked the question that gave this project its name: if the existing processes weren't broken, why fix them? The answer, as it turned out, was compelling.














