Jobs · Quality Assurance · Michigan

Lead Software Verification & Validation Engineer

Actalent · Ann Arbor, MI · 2 wk ago
On-siteQuality Assurance$75–$90/hrFull-time

About the role

Our client, an innovative medical device company in Ann Arbor, Michigan, is seeking a Lead Software Test Verification Engineer to support the verification and validation of software used in life-changing medical technologies. This individual will provide technical leadership for a team of Software Test Engineers and will be responsible for planning, coordinating, executing, and documenting software verification and validation activities throughout the product development lifecycle. The ideal candidate possesses a strong background in medical device software testing, test strategy development, requirements-based testing, and regulatory compliance, along with exceptional communication and leadership skills. This is a highly visible role that will play a critical part in ensuring software quality, product safety, and regulatory compliance during an extensive testing and verification cycle.

Responsibilities

  • Lead and mentor a team of 3 Software Test Engineers, providing technical guidance, prioritization, and support throughout verification activities.
  • Develop, review, and execute comprehensive software verification and validation test plans, protocols, and reports.
  • Coordinate testing activities across multiple projects and product releases.
  • Ensure requirements traceability from software requirements through verification testing and final documentation.
  • Drive execution of functional, integration, system, regression, and performance testing activities.
  • Identify testing risks, gaps, and quality concerns and communicate recommendations to project stakeholders.
  • Review test results, investigate defects, support root cause analysis, and drive issue resolution efforts.
  • Collaborate closely with Software Engineering, Systems Engineering, Quality Assurance, Regulatory Affairs, and Program Management teams.
  • Maintain compliance with FDA regulations, ISO 13485, IEC 62304, and company quality management system requirements.
  • Monitor testing progress, communicate status updates, and present results to leadership and cross-functional teams.
  • Support audit readiness activities and contribute to design verification and validation documentation.
  • Drive continuous improvement initiatives related to testing processes, tools, and methodologies.

Requirements

  • Bachelor's degree in Computer Engineering, Software Engineering, Computer Science, Biomedical Engineering, or related technical discipline.
  • 8+ years of software testing, software verification, or software validation experience.
  • 2+ years of experience leading or mentoring software test engineers.
  • Proven experience developing and executing software verification and validation test plans.
  • Strong understanding of Software Development Lifecycle (SDLC) and Software Test Lifecycle (STLC).
  • Experience working in a regulated medical device environment.
  • Knowledge of FDA Quality System Regulations and medical device development standards.
  • Experience with requirements-based testing and requirements traceability.
  • Strong defect management, troubleshooting, and root cause analysis skills.
  • Excellent written and verbal communication skills.
  • Proven ability to influence cross-functional teams and communicate effectively with technical and non-technical stakeholders.
  • Strong organizational skills and ability to manage multiple priorities in

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