Pharma QA Documentation Specialist (On-Site)

Granules Pharmaceuticals, Inc. is seeking a QA associate for documentation in Manassas, Virginia. This full-time on-site position ensures compliance with cGMP and internal policies, involves managing document control, performing inspections, and training new hires. Applicants must have at least two years of experience in quality assurance in a cGMP-regulated environment and a relevant college degree. Ideal candidates will possess strong communication skills and the ability to manage multiple priorities effectively.
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