How You Will Achieve It:
- Manage receipt, storage, and handling of Quality control samples.
- Ensure training records are updated and correctly filed to reflect current testing capabilities.
- Perform sampling and labeling of materials as per defined procedure and verification of all the equipment/instruments.
- Interpret and evaluate data in terms of accuracy, precision, trends, and potential Good Manufacturing Practices (cGMP) impact and recommend appropriate corrective actions.
- Ensure all documentations and quality records are conducted in accordance with Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance with existing policies.
- Review and revise Standard Operating Procedures (SOPs), analytical methods, and related procedures/documents, to keep them current.
- Perform analyses on finished products, raw materials, packing materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
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