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Join a team of engineers solving real-world validation challenges for pharma, biotech and life sciences — on a platform built to 21 CFR Part 11, EU Annex 11 and GAMP 5.
Why KOŚA
At Qualify IT Solutions you will help shape KOŚA — our GxP software platform for document control, training, quality and validation. You will write production code for regulated pharma customers, work with senior engineers on architecture, and see your features stand up to real audits.
We invest in our people with continuous training, mentorship and certifications — and we keep teams small enough that your work is visible.
Own regulated modules end-to-end and grow into architecture and lead roles as the platform expands.
Funded GxP, GAMP 5 and CSV learning paths, plus mentorship from engineers who built KOŚA.
A collaborative, respect-driven engineering culture where precision is valued over heroics.
Every release supports patient safety through validated, audit-ready pharma systems.
Open positions
Three openings on the KOŚA engineering team, all onsite at our Nizampet, Hyderabad office.
Own the end-to-end delivery of KOŚA — architecture, AWS EKS migration, GxP compliance reviews and the engineering team.
Own features end-to-end across DMS, LMS and Active Directory modules — schema to React UI, with a compliance-first mindset.
Write production code for a live regulated pharma platform, with priority consideration for a full-time Junior Developer role.
