R&D
Equipment and Facilities
Name:QA Department
Description:QA Department has broad responsibilities and authority in the following areas: - 1.Quality Improvement- Quality improvement is based on the premise that all work activities can be planned, performed, measured, and improved. QA monitors our progress toward our corporate goal of building a culture in which improvement is continuous and an integral part of the organization. QA department is making efforts to improve quality system continuously to provide the highest quality products and services to domestic and international customers. - 2.Personnel GMP Training and Qualification - all employees who come into contact with our products must begin GMP training within the first month of employment, GMP training continues on a regular basis throughout the length of employment. Tests are given to monitor the effectiveness of training. - 3.Internal Audits - QA inspectors monitor all phases of production to assess performance and adherence to GMP and to the SOPs of each department. - 4.External Audits - QA oversees and supervises inspections and audits of our facilities by domestic and international regulatory bodies, as well as by customers and independent auditing firms. - 5.Supplier Qualification - QA department maintains an audit program to verify our suppliers' ability to provide consistent products that meet our strict quality requirements. - 6.Document and Record Control - QA is responsible for maintaining all documents, records and Standard Operating Procedures, making sure that they are up to date. - 7.Inspection and Acceptance Testing - QA has the authority to release and reject any component or finished product that does not meet specifications. - 8.Non-Conformances - QA handles the identification, documentation, control, investigation and disposition of all non-conforming materials, components and final products
Description:QA Department has broad responsibilities and authority in the following areas: - 1.Quality Improvement- Quality improvement is based on the premise that all work activities can be planned, performed, measured, and improved. QA monitors our progress toward our corporate goal of building a culture in which improvement is continuous and an integral part of the organization. QA department is making efforts to improve quality system continuously to provide the highest quality products and services to domestic and international customers. - 2.Personnel GMP Training and Qualification - all employees who come into contact with our products must begin GMP training within the first month of employment, GMP training continues on a regular basis throughout the length of employment. Tests are given to monitor the effectiveness of training. - 3.Internal Audits - QA inspectors monitor all phases of production to assess performance and adherence to GMP and to the SOPs of each department. - 4.External Audits - QA oversees and supervises inspections and audits of our facilities by domestic and international regulatory bodies, as well as by customers and independent auditing firms. - 5.Supplier Qualification - QA department maintains an audit program to verify our suppliers' ability to provide consistent products that meet our strict quality requirements. - 6.Document and Record Control - QA is responsible for maintaining all documents, records and Standard Operating Procedures, making sure that they are up to date. - 7.Inspection and Acceptance Testing - QA has the authority to release and reject any component or finished product that does not meet specifications. - 8.Non-Conformances - QA handles the identification, documentation, control, investigation and disposition of all non-conforming materials, components and final products
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Company Info
Miracle International Trading Co., Ltd.
[China]
[Verified Member]
Online Postings: Products
Business Type:Manufacturer, Trading Company, Business Service (Transportation, finance, travel, Ads, etc), Other
City: Guangzhou
Province/State: Guangdong
Country/Region : China
