2 of 2 Permanent Risk Analysis Jobs in Motherwell

cases against embedded medical-device software. Produce documented verification and validation evidence. Report, investigate and manage software defects through to resolution. Contribute to impact analysis, risk analysis and FMEAs. Manage testing priorities using Jira sprint boards. Support regulatory submission and commercial release deadlines. Essential experience Personally writing … software embedded within a medical device. Medical-device software V&V within a regulated development environment. Documenting test results and linking evidence to requirements. Risk-based testing and contribution to risk-management activities. Leading testing activities while remaining hands-on. Experience supporting an FDA 510(k) submission ...

ensure V&V evidence supports FDA 510(k) submissions and commercial software releases. You will collaborate with regulatory teams, manage defects, and contribute to risk analyses while driving testing priorities in Jira. Experience with medical-device validation is essential. #J-18808-Ljbffr ...