Description:
job summary: We are looking for a Document Control Specialist with experience in the FDA industry either with a biotech, pharma or medical device company. Candidate will be working to streamline documents from several quality management systems including Oracle (lot traceability), Maximo, Labvantage and Master Control. Our Technical Writer/Document Controller will Manage the current document control system, which contains Policies, Standard Operating Procedures (SOPs), Work Instructions, Templa
Apr 11, 2024;
from:
dice.com