DevOps Engineer – Medical Devices (f/m/x)
In short
DevOps Engineer needed for medical device software development in Szczecin. Tasks include CI/CD pipeline design/maintenance, automation, and regulatory compliance. Requires 5+ years DevOps exp, knowledge of medical device standards (IEC 62304), Azure DevOps, YAML, Git, DevSecOps, and regulatory frameworks (FDA, EU MDR). Fluent English and Polish required.
AI-written summary based on the listing content.
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
| Published | 2026-07-06 |
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