Receive and archive the production documentation , including the Batch Record and COA.

及时准确接收、存入各种与生产有关原始记录.

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Be responsible for routine production packaging batch record creation and maintenance.

负责试日常生产批次包装批记录编写与维护.

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Fill in batch record and other documents truly and timely.

真实地及时地填写批生产记录和其他文件.

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To file the batch record in the GMP library termly.

将批记录定期归档在GMP图书馆.

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Documentation. Fill in the information for batch record, logbook and other record.

文件完整, 准确和及时地填写批次记录, 日志和其他记录.

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Fill in the information for batch record, logbook and other record.

完整,准确和及时地填写批次记录, 日志和其他记录.

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The Batch record is verified and authorized by the Quality Assurance Manager.

由品质经理检验并授权记录批号.

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Running manufacture order and prepare batch record.

下达生产订单并准备批生产记录.

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All tests and results should be fully documented as part of the batch record.

所有的检测和结果应全部记录作为批记录的部分.

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Be responsible for trial batch and routine production batch record creation and maintenance.

负责试制批次与日常生产批次批记录编写与维护.

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Review and check batch documentation assure the accuracy and integrity of information in batch record.

审核批生产记录,确保批记录准确完整.

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All test and results should be fully documented as part of the batch record.

所有测试及结果都应当作为批记录的一部分全部归档.

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Review batch record before release, to ensure product releasing meet the SOP requirement.

产品放行前批档案审核, 保证产品放行符合规范要求且无失误.

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