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