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Global Quality Documentation Lead
Job in
Columbia, Lexington County, South Carolina, 29228, USA
Listed on 2026-07-13
Listing for:
Otsuka America Pharmaceutical Inc.
Full Time
position Listed on 2026-07-13
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
Otsuka America Pharmaceutical Inc. in the United States seeks a Quality Documentation Specialist to manage global, regional, and local procedural documents and governance activities.
You will support inspections, regulatory intelligence, validation, and project liaison activities while promoting continuous improvement of the Quality System and alignment with global SOPs and policies. The role requires collaboration with global quality leads and cross-functional teams to ensure training readiness
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