QA Documentation Specialist – Pharma (cGMP)

A pharmaceutical company is seeking a QA Associate for documentation to ensure compliance with cGMP and internal policies. The role involves managing document control systems, conducting inspections, and performing quality system functions. The ideal candidate has at least two years of experience in a quality assurance role within a cGMP-regulated environment and holds a degree in a science-related field. Strong communication skills and the ability to prioritize tasks are essential for this position set in Manassas, Virginia.
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