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Seeking a QA Document Control Specialist to manage documentation processes in a cGMP-regulated pharmaceutical setting. The role involves organizing indexing archiving and retrieving quality records while supporting audits and inspections.
Key Responsibilities:Organize and index QA documents across departments
Manage offsite storage (including coordination with vendors like Iron Mountain)
Maintain document retrieval logs and audit readiness
Track and log document requests; manage check-outs and sign-offs
Support during FDA or internal audits/inspections
Associates degree (AS) or equivalent experience in pharmaceutical/life sciences documentation
1 3 years QA experience working with documentation systems in a cGMP environment
Must be able to read and speak English fluently
Full-time