QA Associate I — GMP Compliance & Process Improvement
ProQuality Network
ProQuality 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 TrackWise, and training of manufacturing staff; requires a Bachelor’s or HS with experience. #J-18808-Ljbffr ProQuality Network
Vacancy posted 5 days ago
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