Senior Software Test Engineer (Medical Devices)

Siemens Healthineers AG

Walpole (MA)

On-site

USD 106,000 - 145,000

Full time

4 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k) retirement plan
Life insurance
Disability insurance
Paid parking/public transportation
Paid time off
Paid sick time

Job summary

Siemens Healthineers AG in the United States is seeking a Senior Software Test Engineer to independently plan and execute verification/validation activities for medical device software. You will design, develop and run tests, manage defect tracking, and provide objective evidence that requirements are met while collaborating across project teams.

The role requires experience with regulated software development, risk management, and design controls, plus familiarity with automated testing and

Qualifications

  • Experience in verifying and validating software in a regulated environment for medical devices.
  • Ability to create and execute comprehensive test plans and tests from requirements.
  • Familiarity with risk management and design control processes.

Responsibilities

  • Design, develop and execute software tests to verify the design meets requirements.
  • Plan and implement configuration of physical equipment setups.
  • Track defects in a defect tracking system and support root-cause analysis.
  • Report test results to the test team lead and project manager.
  • Generate evidence that requirements are satisfied by design outputs.
  • Communicate task status and software quality across teams.
  • Collaborate with project teams and grow into a product subject matter expert.

Skills

Black-box testing
Performance testing
Automated testing
Manual testing
CI/CD
Azure DevOps
Python
C#
Java
JavaScript/TypeScript
Requirements analysis
Root cause analysis
Test planning

Education

BS/MS in Computer Science or Engineering

Tools

Defect tracking system

Job description

Siemens Healthineers AG in the United States is seeking a Senior Software Test Engineer to independently plan and execute verification/validation activities for medical device software. You will design, develop and run tests, manage defect tracking, and provide objective evidence that requirements are met while collaborating across project teams.

The role requires experience with regulated software development, risk management, and design controls, plus familiarity with automated testing and

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