Roles & ResponsibilitiesDescription:Quality Engineer RoleLooking for Class II Medical Device experience performing Design Transfer activities per FDA CFR 820. Primary responsibilities will be Test Method Validations, Analysis with Minitab Software, IQ/OQ/PQ, Non-Product Software Validation, PFMEA, DFMEA, in accordance with ISO 14971, ISO 13485.Experience RequiredSkills & CertificationsEligibilities & qualifications.