Medical Device Test Architect

Axiom Global Technologies

Andover (MA)

On-site

USD 140,000 - 190,000

Full time

2 days ago
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Job summary

Axiom Global Technologies in Andover, MA is seeking an experienced Test Architect to lead backend testing strategy and automation for a healthcare technology platform. You will design end-to-end test frameworks, develop SVPs compliant with FDA standards, and oversee API, microservices, database, performance, and security testing.

This role integrates testing into CI/CD pipelines and focuses on risk-based testing, metrics, and formal test documentation, collaborating with architecture,

Qualifications

  • 9–13 years of overall experience, including 3+ years in Test Architecture.
  • Strong background in FDA-regulated medical device software.
  • Hands-on experience with Software Verification & Validation (V&V).
  • Experience mentoring QA/Test Engineering teams.

Responsibilities

  • Design end-to-end test automation frameworks.
  • Develop Software Verification Plans (SVP) aligned with FDA standards.
  • Lead API, microservices, database, performance, and security testing.
  • Integrate automated testing into CI/CD pipelines.
  • Drive risk-based testing, quality metrics, and test documentation.
  • Collaborate with architecture, cybersecurity, and DevSecOps teams.

Skills

Backend automation
API testing
Test architecture
CI/CD integration
Security testing

Tools

CI/CD tooling
API testing frameworks

Job description

We are looking for an experienced Test Architect to lead backend testing strategy and automation for a healthcare technology platform.

Key Responsibilities:
  • Design end-to-end test automation frameworks.
  • Develop Software Verification Plans (SVP) aligned with FDA standards.
  • Lead API, microservices, database, performance, and security testing.
  • Integrate automated testing into CI/CD pipelines.
  • Drive risk-based testing, quality metrics, and test documentation.
  • Collaborate with architecture, cybersecurity, and DevSecOps teams.
Required Experience:
  • 9-13 years of overall experience, including 3+ years in Test Architecture.
  • Strong background in FDA-regulated medical device software.
  • Hands-on experience with Software Verification & Validation (V&V).
  • Expertise in backend automation, API testing, and CI/CD.
  • Knowledge of medical device regulations and cybersecurity practices.
  • Experience mentoring QA/Test Engineering teams.
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