Assess manufacturers' software lifecycle processes and technical documentation for medical device software, including SaMD and AI-enabled devices, under EU MDR, UK MDR, and relevant IEC standards. Raise and close out technical assessment findings with manufacturers, explaining regulatory requirements clearly and constructively. Deliver consistent, high-quality assessments that match Scarlet's methodology and values, working independently with flexible scheduling. #J-18808-Ljbffr
Product Reviewer - Contractor (Fully Remote) in workfromhome at Unknown Company
This position is listed as full time and onsite.