Build the future of pharma
Compliance.

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

Real projects. Real impact.
Real growth.

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.

Career growth

Own regulated modules end-to-end and grow into architecture and lead roles as the platform expands.

Continuous learning

Funded GxP, GAMP 5 and CSV learning paths, plus mentorship from engineers who built KOŚA.

People first

A collaborative, respect-driven engineering culture where precision is valued over heroics.

Work that matters

Every release supports patient safety through validated, audit-ready pharma systems.

Open positions

Find your role

Three openings on the KOŚA engineering team, all onsite at our Nizampet, Hyderabad office.

Senior Full Stack Engineer & Tech Lead

Own the end-to-end delivery of KOŚA — architecture, AWS EKS migration, GxP compliance reviews and the engineering team.

Mid-Level Full Stack Developer

Own features end-to-end across DMS, LMS and Active Directory modules — schema to React UI, with a compliance-first mindset.

Full Stack Developer Intern

Write production code for a live regulated pharma platform, with priority consideration for a full-time Junior Developer role.

Build the future of pharma Compliance.

Real projects. Real impact. Real growth.