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Quality Control Manager (Pharmaceutical Industry)

To ensure the quality of raw materials, packaging materials and finished products are compliant with the approved specifications and GMP/GLP.Maintains a controlled documentation system in the quality control department.Monitors compliance with the requirements of approved procedures.Reviews of quality control records.Ensures that the proper monitoring and the maintenance of department premises and equipment are done properly.Ensures that the Monitoring of the calibration program of equipment is done.Checks the Laboratory organization (For example; document, glassware, chemicals, and equipment).Ensures the organization and proper keeping of retained samples in the retained samples room.Ensures the proper handling of reference and working standards.Ensures the Monitoring of the retention of the QC records.

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