Pharma Documentation Systems Lead; GMP & QA)
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Afton Scientific is seeking a Documentation Systems Specialist III to support our Quality Assurance team. The role focuses on administering master documents and databases to ensure cGMP-compliant documentation and data integrity across pharmaceutical operations.
Key duties include maintaining controlled documents (SOPs, batch records, specifications), reviewing change requests, and supporting audits and VIP visits with meticulous attention to detail.
The Pharma Documentation Systems Lead (GMP & QA) position in the Management & Operations, IT & Technology field is open for applications.
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This posting is for the Pharma Documentation Systems Lead (GMP & QA) role at Virginia Economic Development Partnership, based in Charlottesville, VA, United States.
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