Assistant Document Control needs 1 to 3 years of relevant experience in the pharmaceutical/biopharmaceutical industry Assistant Document Control requires: • BA/BS degree or equivalent experience is preferred. • 1 to 3 years of relevant experience in the pharmaceutical/biopharmaceutical industry is required. • Strong computer applications in the Microsoft Office Suite • Document scanning Assistant Document Control duties: • Assist in the distribution, reconciliation, labeling and filing of GMP documentation. • Update and maintain document tracking databases and archival systems. • Assist in Documentation Audit programs for GMP documents. • Some physical movement of document files/boxes is required; must be able to lift 30 pounds • Distribute approved documentation to appropriate personnel, track receipt of documentation, reconciliation and maintain distribution matrices. • Assist in the maintenance of hard copy and electronic document files. • Label and code files for storage in on-site Documentation Centers. • Assist in the administration of the company GMP Records Retention Policy, including document imaging and preparing documents for shipment to off-site storage. • Data Entry of batch record data into qualified database. 6. Initiate and track periodic Documentation Binder Audits to assure documentation in the field is current and complete. • Ensure ethics and compliance commitment at all times. • Report/Address compliance issues in a timely manner. Attend cGMP training programs as required.