Senior Consultant - MedTech QMS Complaints
Veeva Systems · Minnesota - Minneapolis
8+ years of experience in GMP Systems ownership or Software Consulting; 5+ years of experience in Complaints Management for Medical Device; Strong understanding of FDA, EU MDR/IVDR requirements and Reporting
This posting is pulled directly from Veeva Systems's own Lever page and applying happens on their site, not here. Posted 2025-06-23; Skip The Boards re-checks every company's board regularly and removes listings that disappear from the source.