Tisch
1, responsible for the acceptance of returned drugs purchased by the company after sale and the maintenance of drugs (Chinese herbal medicines, Chinese herbal pieces and finished drugs). Familiar with relevant specifications of Good Manufacturing Practices (gsp).
2. Guide and urge the keeper to store and operate drugs reasonably.
3. Effectively monitor the warehouse temperature and humidity automatic monitoring system.
4. Correct use of maintenance and metering equipment, regular inspection and maintenance to ensure normal operation; Responsible for the annual inspection of measuring equipment
5. Chinese herbal medicines and Chinese herbal pieces should be maintained and recorded by effective methods according to their characteristics, and the maintenance methods adopted should not cause pollution to drugs.
extreme
1. Responsible for making quality management work plan and summary, and assisting department leaders to carry out internal audit and annual external audit.
2. Responsible for assisting department leaders to organize and implement the study and training of system documents.
3. Responsible for assisting department leaders to revise quality management system documents.
4. Responsible for the real-time monitoring of the operational effectiveness of the department system.
5. Be responsible for the statistics, analysis and feedback of data related to the operation of the quality management system of this department.
6. Be responsible for tracking and verifying nonconformities.
Tisso
1, to guide and urge warehouse personnel to store and operate drugs reasonably;
2. Check and improve the storage conditions, protective measures and sanitary environment;
3. Effectively monitor and control the temperature and humidity of the warehouse, dynamically monitor and control the temperature and humidity of the warehouse, and take corresponding measures such as ventilation, cooling and dehumidification according to the changes of temperature and humidity to control the temperature and humidity to ensure the storage quality of drugs;
4, according to the maintenance plan to check the appearance, packaging and other quality status of the drugs in stock, and establish maintenance records; Varieties with special requirements for storage conditions or short validity period should be maintained; Regularly check the circulation quality maintenance of drugs in stock;
5. Be responsible for the management and maintenance of maintenance instruments and equipment, and establish instruments and equipment management files;
6. Correct use of storage and metering equipment for maintenance, regular inspection and maintenance, and metrological verification and measurement to ensure its normal operation.