Description:
Required: Must have two to four (2-4) years of related work experience in the Medical field.Experience in Quality Engineering.Strong understanding in GMP and/or regulatory requirements, specifically 21 CFR 820, ISO 13485, and ISO 14971.Strong communication, collaboration, and problem-solving skills.Both, FDA, and ISO regulations knowledge.Strong root cause analysis skills. Preferred: Operations supplier quality experience.Experience in the medical device and/or pharmaceutical industry.FDA CFR P
Apr 24, 2024;
from:
dice.com