Description:
Skills: CSV, SDLC, CCB, IQ, URS, SDS and RTM, Software, Quality, SQE Experience (Years): 4-6 Essential Skills: Working knowledge of FDA and European medical device regulations (QSR and ISO) is required. Working knowledge of software validation requirements for software used in the production of medical devices and software used to support the Quality System is required. Working knowledge of GAMP5 and SDLC is required. Working knowledge of regulations for electronic records, electronic signat
Jul 21, 2025;
from:
dice.com