Hybrid Firmware Test Engineer - Medical Devices

Actalent

Osseo (MN)

Hybrid

USD 69,000 - 76,000

Part time

8 days ago
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Job summary

Actalent in Maple Grove, MN is seeking a hands-on Firmware Test Engineer to lead verification and validation for a Class III medical device program. You will develop, execute, and maintain firmware verification tests and ensure requirements traceability throughout final stages of product development.

This contract role is onsite in Osseo/Maple Grove, MN with hybrid expectations. You will review verification plans, author DHF documents, perform risk-based testing, support FDA submissions, and

Qualifications

  • Experience testing firmware for embedded devices.
  • Ability to derive test cases from requirements.
  • Knowledge of regulated environments.
  • Experience with DHF documentation.
  • Strong documentation and communication skills.

Responsibilities

  • Execute firmware verification and validation for a regulated medical device.
  • Review and update verification plans and test protocols.
  • Create DHF docs: Verification Plans, Test Protocols, Test Reports.
  • Ensure requirements-to-test-to-results traceability.
  • Perform manual firmware and system-level testing.
  • Conduct risk-based testing aligned with medical device standards.
  • Participate in risk assessments and mitigations.
  • Support FDA submission readiness and compliance.
  • Investigate test failures and drive root-cause analysis.
  • Support commercialization and remediation efforts.
  • Help develop scalable verification processes and team expansion.

Skills

Firmware testing
Embedded systems testing
Verification & validation
Requirements traceability
Risk-based testing
Technical writing

Job description

Actalent in Maple Grove, MN is seeking a hands-on Firmware Test Engineer to lead verification and validation for a Class III medical device program. You will develop, execute, and maintain firmware verification tests and ensure requirements traceability throughout final stages of product development.

This contract role is onsite in Osseo/Maple Grove, MN with hybrid expectations. You will review verification plans, author DHF documents, perform risk-based testing, support FDA submissions, and

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