QA Auditor : GMP & In-Process Quality
Listed on 2026-11-01
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Production QC/QA
Aveva Drug Delivery Systems Inc. is seeking a Quality Assurance In-Process (QAIP) Auditor I to support Manufacturing, Packaging, R&D, and QC operations by performing line clearance, visual inspection of finished products, and sampling from the production line.
The role includes on-line batch record review, AQL planning, QA envelope documentation, and collaboration with Production to resolve quality issues while maintaining GMP compliance and adherence to Aveva SOPs.
Step into the QA Auditor I: GMP & In-Process Quality role at Aveva Drug Delivery Systems Inc in FL, United States and grow with us.
We invite applications for the QA Auditor I: GMP & In-Process Quality position located in FL, United States.
The following opportunity is for a QA Auditor I: GMP & In-Process Quality with Aveva Drug Delivery Systems Inc.
Our organisation is growing, and we are hiring a QA Auditor I: GMP & In-Process Quality in FL, United States.
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