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

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

Sii Sp. z o.o.

Hybrid
B2B

Hexjobs Insights

DevOps Engineer role focusing on CI/CD pipelines for medical devices. Requires 5+ years experience in regulated environments and knowledge of various compliance standards. Benefits include profit sharing and growth investments.

Schlüsselwörter

CI/CD
VectorCAST
SonarQube
Black Duck
unit testing frameworks
DevSecOps
regulatory compliance
medical devices
SOP

Vorteile

  • Great Place to Work since 2015
  • Stable employment
  • Profit sharing with workers
  • Attractive benefits package including healthcare
  • Comfortable workplace options
  • Financial support for employee ideas
  • Investment in personal growth

Technologies we use

About the project

Your responsibilities

  • 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

Our 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

This is how we work on a project

What we offer

  • 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
Aufrufe: 1
Veröffentlichtvor 3 Tagen
Läuft abin 27 Tagen
Art des VertragsB2B
ArbeitsmodusHybrid

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