Verification and Validation Engineer
MDAEdge · West Pittsburg, PA · 1 mo ago
On-siteEngineeringFull-time
Job Summary
You will work as a V&V Lead to coordinate all V&V activities necessary to support the release of new and updated medical devices. Focus will be assessing and testing the requirements of electromechanical medical devices at the system, sub-system, and part level; examples include ventilators, sleep therapy devices, oxygen concentrators, personal wellness devices, and the accessories necessary for proper functionality of these types of devices.
Roles & Responsibilities
- Learn from and adhere to internal quality manual (Quality System Procedures, Work Instructions, Forms).
- Interact with cross-functional project teams to provide inputs to project plans and schedules.
- Estimate resource needs for project support.
- Review requirements and scrutinize for testability.
- Develop V&V test plans, test procedures, requirements trace matrices, and test reports.
- Assign project tasks and responsibilities to V&V team.
- Act as advisor to team to meet schedules and solve technical problems.
- Quickly learn to use automated test tools and specialty test equipment; develop and validate Client test methods (TMV, DOE, Gage R&R studies).
- Execute test procedures both personally and using test technicians.
- Log defects and issues found during V&V activities and track to closure.
- Participate in defect review boards.
- Perform regression analysis and determine testing associated with design changes.
- Plan and facilitate V&V formal technical review and design review meetings.
- Provide weekly project status reports.
- Prioritize project tasks to complete on schedule while maintaining quality of work.
- Work in a team environment; peer review work.
- Work on multiple, concurrent projects.
Minimum Qualifications
- Bachelor's Degree in an engineering discipline; electrical engineering or mechanical engineer background preferred.
- 5 years professional experience in the medical device industry.
- Working knowledge of global medical device regulations, requirements, and standards.