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

Poznań
Białystok
Wrocław
Łódź
+10
Läuft ab 4 Okt 2026
vor 2 Monaten

Kurzfassung

DevOps Engineer for medical device software in Poznań. Design, implement, maintain CI/CD pipelines in Azure DevOps. Requires 5+ yrs exp, IEC 62304/ISO 13485 knowledge, DevSecOps, regulatory compliance (FDA/MDR). Fluent English & Polish.

Von KI erstellte Kurzfassung des Anzeigentextes.

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 in Azure DevOps or equivalent environments
  • Building and maintaining pipeline-as-code solutions using YAML and integrating automated testing and analysis tools
  • Ensuring CI/CD workflows comply with SOPs and regulatory requirements, including traceability, auditability, and reproducibility
  • Integrating tools such as VectorCAST, SonarQube, Black Duck, and unit testing frameworks into CI/CD processes
  • Collaborating with Software Engineering, QA, and Compliance teams to ensure regulatory alignment and product quality
  • Supporting change control processes and contributing to audit readiness and DHF-compliant documentation
  • Requirements
  • Minimum 5 years of experience in DevOps/CI/CD engineering, preferably in regulated or safety-critical environments
  • Hands-on experience with medical device software development standards (e.g., IEC 62304, ISO 13485, or equivalent)

Strong experience with CI/CD tools (preferably Azure DevOps) and pipeline-as-code (YAML)

Proficiency in Git-based workflows, branching strategies, and distributed version control systems

  • Knowledge of DevSecOps practices, including IAM, secrets management, and secure CI/CD designVery good understanding of regulatory frameworks (FDA 21 CFR Part 820, EU MDR) and change control processes
  • Fluent English, both written and spoken
  • Fluent Polish required
  • Residing in Poland required
Veröffentlicht 2026-07-06
Quelle