Medical Device Verification Engineer

Actalent; Plymouth (MN); On-site; USD 58,000 - 82,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability coverage

Health Spending Account (HSA)

Paid Time Off

Job summary

Actalent in Plymouth, MN seeks a Software Test Engineer to execute system-level verification for a regulated medical device platform. You will author test scripts, validate builds on target hardware, and generate audit-ready documentation within a regulated DHF process.

This onsite role offers exposure to the full verification lifecycle and FDA-regulated development practices. Approximately 70% of time is hands-on testing, with 30% focused on verification reporting and documentation.

Qualifications

• Bachelor's degree in engineering or computer science.
• Minimum 2 years in software testing, verification, or related roles.
• Experience writing test scripts for medical/device software.
• Experience authoring verification documents.
• Familiarity with DHF documentation process.
• Ability to collaborate with software engineers for test coverage.

Responsibilities

• Author system-level verification test scripts and protocols using ALM-based processes.
• Install and configure software releases on designated embedded hardware platforms.
• Execute scripted verification testing to confirm system behavior against requirements.
• Perform exploratory verification testing to identify edge cases.
• Maintain end-to-end traceability between requirements, test cases, and test results.

Skills

C++

Google Test

Test scripting

ALM processes

DOORS

V&V testing

Education

Bachelor's degree in Engineering/CS

Tools

PrisMax

ALM

Job description

Actalent in Plymouth, MN seeks a Software Test Engineer to execute system-level verification for a regulated medical device platform. You will author test scripts, validate builds on target hardware, and generate audit-ready documentation within a regulated DHF process.

This onsite role offers exposure to the full verification lifecycle and FDA-regulated development practices. Approximately 70% of time is hands-on testing, with 30% focused on verification reporting and documentation.