DevOps Engineer – Medical Devices (f/m/x)

We are looking for an experienced DevOps Engineer to join a project delivered for a company in the medical technology industry, developing software for medical devices in a strictly regulated environment.

This is a role for a specialist who wants to have a real impact on the quality and safety of solutions used in the healthcare sector.

Your tasks

• Designing, implementing, and maintaining automated CI/CD pipelines for medical device software

• Configuring CI/CD processes in alignment with Software Workflow Standard Operating Procedures (SW SOP)

• Integrating and configuring tools such as VectorCAST, SonarQube, Black Duck, and unit testing frameworks (e.g., xUnit)

• Ensuring compliance of CI/CD processes with regulatory requirements, including traceability, reproducibility, and audit readiness

• Collaborating with Software, QA, and Compliance teams to ensure quality and regulatory alignment

• Supporting change control processes and contributing to audit and regulatory readiness activities

Requirements

• At least 5 years of experience in designing and implementing CI/CD pipelines, preferably in regulated environments

• Hands-on experience with medical device software development processes (e.g., IEC 62304, ISO 13485 or equivalent)

• Strong knowledge of SOP-driven workflows and experience working strictly according to approved procedures

• Practical experience with tools such as VectorCAST, SonarQube, Black Duck, and unit testing frameworks (e.g., xUnit)

• Solid understanding of DevSecOps practices and CI/CD for embedded or safety-critical systems

• Familiarity with regulatory requirements (e.g., FDA 21 CFR Part 820, MDR) and change control processes

• Very good command of English (both written and spoken)

• Fluent Polish required

• Residing in Poland required