The quality manager needs to keep quality records, organize, archive and promptly summarize and report the records; the following are the job responsibilities of the quality manager that I have carefully collected and organized. I will share them with you below. Enjoy it.
Quality Manager Job Responsibilities 1
1. Responsible for collecting the qualification certificates of upstream and downstream customers, entering the collected qualification information data into the system, and at the same time dynamically managing customer qualifications;
2. Responsible for the review of the first-run variety information, and code the qualified first-run variety information according to the coding principles established by the company to ensure that the information is accurate;
3. Responsible for the company’s qualifications , entrusted issuance;
4. Responsible for collecting drug quality information, timely analysis, processing, transmission and feedback;
5. Responsible for drug quality consultation, inquiries, complaints and quality incidents Investigation, processing and reporting;
6. Responsible for the review of unqualified drugs and supervision of the processing process of unqualified drugs;
7. Responsible for collecting and keeping the quality data of the department , files, and urge each position to prepare various ledgers and records;
8. Complete other tasks assigned by superior supervisors.
Quality Manager Job Responsibilities 2
1. Responsible for the organization and archiving of various quality files (including quality ledgers, records, supplier and customer files, product files, etc.) Work.
2. Responsible for handling medical device quality inquiries, answering quality issues and keeping records.
3. Responsible for reviewing the qualifications of medical device suppliers, products, and purchasers for the first cooperation, and uploading relevant qualifications.
4. Supervise the judgment of medical device products by the warehouse entry acceptance post and the warehouse review post
5. Responsible for the supervision of the processing process of unqualified medical devices and keep relevant records .
6. Cooperate with the Ministry of Commerce and Technical Services Department to carry out user interviews and customer satisfaction surveys, and establish relevant files.
7. Responsible for the processing and reporting of adverse reaction information of medical devices.
8. Responsible for collecting and analyzing medical device quality information and providing feedback.
9. Leaders arrange other work
Quality Manager Job Responsibilities Part 3
- Responsible for medical device product quality management documents, and guide and supervise the execution of the documents and management;
-Responsible for the operation and maintenance of the medical device quality management system (ISO9000); proposing and implementing improvement measures to improve product quality;
-Responsible for establishing the medical equipment operated by the company Quality files for device products and including quality acceptance standards;
- Responsible for the quality inquiry and declaration of adverse events of medical device products in the hospital Red Cross System and the Food and Drug Administration website;
-Assist in education and training on medical device product quality management;
-Execute warehouse quality management processes and improve warehouse quality management methods;
-Provide comprehensive quality analysis reports to evaluate products Quality status, control of unqualified products;
- Incoming goods inspection, outgoing inspection, verification and handover; sorting and archiving of relevant purchase, sale and inventory records;
Quality manager Job Responsibilities Chapter 4
1. Responsible for on-site inspection and on-site quality supervision and management of production (including external workers);
2. Responsible for the acceptance and random inspection of raw materials and finished products.
3. Responsible for medical laboratory quality control and on-site quality supervision and management;
4. Responsible for document management and archive management related work;
5. Other tasks assigned by the person in charge of the quality control department.
Quality Manager Responsibilities Part 5
1. Participate in the preparation and revision of relevant documents of the quality management system.
2. Participate in the maintenance, supervision, inspection, and tracking verification of the daily operation of the quality management system.
3. Responsible for the archiving of quality management system-related documents and the collection and preservation of quality system operation records.
4. Participate in the preparation of internal audit plans, organize internal auditors to conduct audits according to plan requirements, and track and verify the implementation effects of corrective measures.
5. Participate in the preparation work before external audits, promote the rectification and tracking of audit issues, and ensure that audit issues are closed in a timely and effective manner.
6. Responsible for regularly updating and collecting laws and regulations related to the system.
Quality Manager Job Responsibilities Part 6
1. Assist in maintaining and improving the company's quality assurance system to ensure its normal operation;
2. Responsible for organizational process analysis and process optimization;
3. Responsible for following up and guiding the specific work that needs improvement and rectification for quality system improvement;
4. Responsible for the overall arrangement of quality system certification and audit-related work;
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5. Customer satisfaction survey return visit, complaint handling;
Quality Manager Responsibilities Part 7
1. Develop quality management standards;
2. Standardize the quality control process and supervise each quality node;
3. Organize quality audits, including quality: light inspection, random inspection, etc.;
4. Collect and organize quality system records ;
5. Develop quality management training and implementation;
6. Formulate and promote product standards, certification and other detailed rules;
7. Preparation and implementation of product certification materials Handle;
8. Supervise and verify the reasonable operation of the company's quality management system and continue to improve;
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