Description:
JOB DESCRIPTION: Quality Engineering with focus on Design Improvements Develop knowledge with the following regulations and standards: o 21 CFR Part 820 Medical Device Quality System Regulations (QSR) o ISO 13485:2016 Medical devices Quality management systems o EN ISO 11135-1:2007 Sterilization of healthcare products Ethylene Oxide o EU Medical Device Regulation Assist in Non-Conforming material resolution including root cause investigation and communication with suppliers. Assist in Corrective
Apr 8, 2024;
from:
dice.com