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Coordinator, QA Document Control
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Full-time
- The Quality Document Control Coordinator will be responsible for the supporting review of Master Manufacturing Records (MMRs); review of Receipt of Goods documentation; review of manufacturing and packaging work orders, quality inspection data, certificates of analysis, reprocessing orders, and deviations as relate to production in under both food and dietary supplements regulation.
- Provide customer service to all employees needing assistance with GMP, GDP and GLP controlled documentation.
- Knowledge of basic GMP and QA/QC in the food, nutraceutical or pharmaceutical industry
- A minimum of two years’ experience in QA/QC
- Previous experience as a team member of Quality Compliance ASQ, Six Sigma, or applicable certifications
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