Demo

Assistant Document Control

Global Channel Management
Somerville, NJ Full Time
POSTED ON 1/22/2025
AVAILABLE BEFORE 4/22/2025

About the job Assistant Document Control

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.
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