DevOps Engineer – Medical Devices (f/m/x)
Коротко
DevOps Engineer for medical device software in Lublin. Design/maintain CI/CD pipelines (Azure DevOps, YAML), integrate tools (VectorCAST, SonarQube), ensure regulatory compliance (IEC 62304, ISO 13485). Req: 5+ yrs DevOps, medical device standards, Git, DevSecOps, regulatory frameworks. Fluent English & Polish.
Ключові слова
Стислий виклад підготував ШІ на основі тексту оголошення.
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
| Опубліковано | 2026-07-06 |
| Джерело |
|
Hexjobs App
Інструменти, налаштовані під цю вакансію.
Hexjobs App
Інструменти, налаштовані під цю вакансію.