Pharma Tech Full-Stack Software Developer

F. Hoffmann-La Roche AG; Warszawa; On-site; PLN 112,000 - 201,000; Full time

Benefits offered by this job

Annual bonus

Training budget

Recharge Fridays

Take Time Program

Vacation subsidy

Flex Location

Take Time for Charity

Private healthcare

Group life insurance

Stock purchase plan

Laptop and car programs

Job summary

Roche is seeking a Custom Software Developer within Pharma Technical Development to contribute across the full software lifecycle. You will build and maintain digital solutions supporting our clinical pipeline and manufacturing processes, ensuring code quality and compliance in a regulated biotech environment.

Collaborating across R&D and PTD, you will develop robust manufacturing and quality systems, leveraging modern stacks and CI/CD pipelines while engaging with internal platforms and

Qualifications

• Active project contributor in software engineering with a focus on delivering software solutions.
• Experience delivering tasks reliably within a structured team environment and understanding of regulatory frameworks (e.g., GxP).
• Ability to execute development plans and participate in knowledge sharing initiatives.

Responsibilities

• Scope / content leadership: design, code, test, and deploy web apps and microservices for PTD.
• Problem solving: contribute features, fix issues, perform peer reviews, communicate risks.
• Stakeholder management: engage with owners, leads, and end users to clarify requirements.
• Impact/Strategy: develop technical skills, pursue trainings, participate in CoEs and CoPs.
• Product size: work on individual features and components within well-defined projects.
• Business/Technical: map components to larger systems and suggest improvements.

Skills

Python

Java

Node.js

TypeScript

React

Angular

Tools

RESTful APIs

SQL

CI/CD

Git

Containerization

Job description

Roche is seeking a Custom Software Developer within Pharma Technical Development to contribute across the full software lifecycle. You will build and maintain digital solutions supporting our clinical pipeline and manufacturing processes, ensuring code quality and compliance in a regulated biotech environment.

Collaborating across R&D and PTD, you will develop robust manufacturing and quality systems, leveraging modern stacks and CI/CD pipelines while engaging with internal platforms and