Description:
QA Document Control Specialist Duration: 10 Months+ Work location: Philadelphia, Pennsylvania Description Primary Duties The QA Document Control Specialist will work to develop, deploy, and support the Veeva Quality Document System, manages, and tracks all GMP documentation. Following Spark SOPs, the incumbent is responsible for adhering to the Spark document lifecycle procedures and archives all records in accordance with the records retention schedule, as well as retrieving all documents as re
Feb 3, 2026;
from:
dice.com