QA Associate — GMP Compliance & Process Improvement
Listed on 2026-10-09
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Quality Assurance - QA/QC
Data Analyst, Regulatory Compliance Specialist
Pro Quality Network in Kentucky seeks a QA Associate I to provide quality support for solid oral dosage manufacturing, ensuring compliance with cGMP, CFR, and company SOPs through review of batch records, in-process testing, and real-time monitoring.
Responsibilities include SOP/batch record reviews, real-time audits, environmental monitoring, investigations, deviation reports in Track Wise, and training of manufacturing staff; requires a Bachelor’s or HS with experience.
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This posting is for the QA Associate I — GMP Compliance & Process Improvement role at Pro Quality Network, based in KY, United States.
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