The Document Control Specialist will join Catalent’s Consumer Health team at its approximately 70,000-square-foot Manassas, Virginia facility, which supports dietary supplement and food-safety cGMP operations from early development through commercial manufacturing and packaging. The role creates and maintains Quality System documentation and supports compliance with SQF, the Food Safety Plan (HACCP), and the Food Quality Plan (FQP). It also supports Quality Assurance projects, communicates deviations to management, and contributes to quality standards and continuous improvement. The position is 100% onsite in Manassas, Virginia, with a Monday–Friday schedule from 9:00 a.m. to 5:30 p.m. The specialist prepares and organizes Quality System documents, manages document routing and approvals, performs internal audits, tracks non-conformances and corrective actions, and works with Production, Packaging, and R&D. The role also includes reviewing operator paperwork, entering and tracking data, following applicable FDA and cGMP standards, and completing required training.
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Job Type
Full-time
Education Level
High school or GED