DevOps Engineer – Medical Devices (f/m/x)
⚲ Białystok, Centrum, Bydgoszcz, Gdańsk, Oliwa, Katowice, Kraków, Podgórze, Lublin, Łódź, Śródmieście, Piła, Poznań, Wilda, Rzeszów, Szczecin, Toruń, Warszawa, Mokotów, Wrocław, Fabryczna
Do uzgodnienia
Wymagania
- IEC 62304
- SOP Development
- SonarQube
- AzureDevOps
- Git
- Bitbucket
- Jenkins
- YAML
Opis stanowiska
Nasze wymagania:
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 design
Very 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
O projekcie:
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.
Zakres obowiązków:
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
Oferujemy:
Great Place to Work since 2015 - it’s thanks to feedback from our workers that we get this special title and constantly implement new ideas
Employment stability - revenue of PLN 2.1BN, no debts, since 2006 on the market
We share the profit with Workers - over PLN 76M has already been allocated for this aim since 2022
Attractive benefits package - private healthcare, benefits cafeteria platform, car discounts and more
Comfortable workplace – class A offices or remote work
Dozens of fascinating projects for prestigious brands from all over the world – you can change them thanks to Job Changer application
PLN 1 000 000 per year for your ideas - with this amount, we support the passions and voluntary actions of our workers
Investment in your growth – meetups, webinars, training platform and technology blog – you choose
Fantastic atmosphere created by all Sii Power People
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 design
Very 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
O projekcie:
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.
Zakres obowiązków:
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
Oferujemy:
Great Place to Work since 2015 - it’s thanks to feedback from our workers that we get this special title and constantly implement new ideas
Employment stability - revenue of PLN 2.1BN, no debts, since 2006 on the market
We share the profit with Workers - over PLN 76M has already been allocated for this aim since 2022
Attractive benefits package - private healthcare, benefits cafeteria platform, car discounts and more
Comfortable workplace – class A offices or remote work
Dozens of fascinating projects for prestigious brands from all over the world – you can change them thanks to Job Changer application
PLN 1 000 000 per year for your ideas - with this amount, we support the passions and voluntary actions of our workers
Investment in your growth – meetups, webinars, training platform and technology blog – you choose
Fantastic atmosphere created by all Sii Power People
🔍 Dekoder Ogłoszenia
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preferably in regulated or safety-critical environments
Doświadczenie w pracy z medycznymi urządzeniami lub podobnymi, gdzie błędy mają poważne konsekwencje, jest preferowane, ale niekoniecznie wymagane.
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have a real impact on the quality and safety of solutions used in the healthcare sector
Twoja praca będzie miała znaczenie, ale może to również oznaczać dużą odpowiedzialność i presję związaną z bezpieczeństwem pacjentów.
🔴
Designing, implementing, and maintaining automated CI/CD pipelines for medical device software
Oczekuje się, że będziesz nie tylko wdrażać, ale także aktywnie projektować i utrzymywać złożone procesy CI/CD w specyficznym, regulowanym środowisku.
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integrating automated testing and analysis tools
Będziesz musiał nie tylko konfigurować narzędzia, ale także rozumieć i integrować różne rodzaje testów i analiz, co może wymagać dodatkowej wiedzy.
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Fluent English, both written and spoken
Jest to standardowe wymaganie, ale w kontekście międzynarodowym i regulowanym, oznacza konieczność płynnej komunikacji w dokumentacji technicznej i dyskusjach.