Quality Management System Staff Job Responsibilities (Selected 21)
As society moves forward step by step, each of us may come into contact with job responsibilities, job responsibilities refers to the content of the specific work of the worker, the responsibility, and to meet the standards required by the superiors, to complete the tasks entrusted to the superiors. So what kind of job duties is effective? The following is my collection of post duties of quality management system clerk (general 16 articles), welcome to share.
Quality management system staff job responsibilities Part 1
1, responsible for the company's production products, sample, batch incoming inspection, strict implementation of acceptance standards, whether the incoming materials qualified to make a clear judgment
2, is responsible for the assembly of the online supervision and inspection, to confirm that the quality of the assembly process in line with the conformity (in line with the drawings, specifications, standards, operating instructions, etc.)
3 Feedback in a timely manner on the inspection process of various types of quality issues, and do the corresponding statistics, records, identification and tracking work
4, according to the inspection list requirements of the final inspection of the finished product to ensure that the finished product meets the relevant requirements
Quality Management System Job Responsibilities Part 21, responsible for the motor electronic control products related to the quality of inspection and record and its related report preparation.
2, responsible for product quality information transfer, quality problem feedback, processing work.
3, responsible for quality issues tracking and resolving, coordinating and coordinating the relevant personnel to rectify and verify.
4, implement and participate in the company's quality system to promote the work requirements.
Quality Management System Staff Job Responsibilities Part 3
1, responsible for automotive parts stamping, welding products related to the inspection work (to determine the potential or has appeared defects);
2, responsible for the site of defective control work;
3, the authenticity of the inspection data, accuracy and completeness of the responsibility;
4, responsible for the work of the site's environmental management and Maintenance and storage of inspection tools.
A production quality inspector job responsibilities:
1, more than 1 year of quality inspector work experience, medical device inspection experience is preferred
2, familiar with the QC inspection techniques and control processes, understanding of ISO9001 quality system
3, Good communication and cooperation spirit, serious and responsible work attitude
Second, the food quality inspector job responsibilities:
Food engineering, can systematically master the inspection process and specification requirements; is responsible for the production process comprehensive quality tracking, to assist in the production plant manager to complete the daily production tasks; to assist in doing a good job the company iso9000 Quality management standards; fully responsible for the work undertaken.
Third, engineering quality inspector job responsibilities:
1, quality inspector license, experience is preferred.
2, careful and rigorous, with good professional quality, team spirit and communication and coordination skills.
3, can adapt to the construction site work outside.
4, strong principles, not afraid to offend people, generous.
Fourth, the mechanical industry quality inspector duties:
Strong sense of responsibility, skilled in the use of various types of gauges, familiar with the drawings, more than 2 years of work experience in the machinery industry.
Quality management system staff job responsibilities Part 5
1, to assist in construction quality verification, review the amount of work;
2, to assist the project manager to do a good job of the project's data collection, storage and archiving;
3, responsible for the project during the construction period of the safety precautions; the quality of the report, the report of the self-inspection before the inspection and inspection and inspection, inspection;
4, reasonable arrangements, scientific Guide, the successful completion of the project's various construction tasks;
5, adhere to the principle of correctly reflecting the quality of the situation, strict quality management;
6, to participate in the completion of the project, responsible for the completion of the project intact protection;
7, the leadership of the other tasks assigned.
Quality management system clerk's job responsibilities Part 6
1, according to the inspection procedures for each process product inspection and record; for each process of the key process parameters for testing and recording;
2, the completion of each process pieces of the inspection in the flow of the card to confirm; the rework of each process / rework pieces of the inspection to confirm and record;
3, for the need to carry out metallographic, hardness For products that require metallographic, hardness and other tests, timely issue a test commission order and send it to the relevant laboratory;
4, should complete the maintenance of test and inspection equipment, test and inspection equipment should be regularly maintained.
Quality management system clerk job responsibilities Part 71, responsible for raw and auxiliary materials, processes, finished products, shipping products and GP12 product inspection, and make a good record of the quality inspection
2, familiar with a variety of inspection tools, and can be used and operated independently
3, through the various "Inspection Specification" to familiarize with the product quality characteristics and acceptance of the standard
4, On the key, special process quality control, inspection and supervision, and deal with process product defects
5, do a good job of testing the status of the product labeling, qualified products, to be confirmed, defective products are summarized and paste the corresponding labels, and records of the inspection, record the record of the form to do a good job of recording
6, to complete the direct superior of the other tasks
quality management system member of the Job responsibilities Part 81, responsible for vehicle maintenance self-inspection, mutual inspection work supervision
2, responsible for Geely Automobile general inspection requirements, the quality of vehicle maintenance of the general inspection work
3, responsible for the quality of vehicle maintenance, statistical records, analysis, and put forward proposals for improvement
4, to assist in the management of the quality file work (the general inspection of the record sheet, the internal return, the return of the sheet)
5, to assist in the management of the quality file work (the general inspection of the record sheet, within the return, etc.)
6, to complete other tasks assigned by the direct superior
5, to assist in the 4S store quality improvement work plan;
6, responsible for assisting the technical director to complete the monthly maintenance quality analysis report and maintenance case preparation and reporting;
7, responsible for participating in the industry's business training and annual audit work;
8, to complete the other work arranged by the higher leadership.
Quality management system staff duties Part 9
1, responsible for the warehouse daily material acceptance quality inspection, warehousing quality inspection, work;
2, responsible for the warehouse daily material review work, the warehouse product total category up to more than 200 kinds of products, need to be familiar with the products in the early stage.
3, responsible for the custody and archiving of relevant documents;
4, warehouse data statistics, archiving, accounting and system data input;
Quality management system staff duties Part 101, responsible for coal, gas, billet and physical and chemical inspection of products.
2, the specimen to be tested should be carefully checked and the accuracy of the test should be ensured.
3, according to the relevant procedures for the preparation of drugs, and routine savings to prevent waste.
4, maintenance of equipment and chemical test supplies.
5, the timely issuance of chemical test report, in the chemical test failed to prompt and feedback to the quality control department.
6, good chemical test records.
7, improve the health and safety of the laboratory operation.
8, to ensure the accuracy of the physical and chemical testing of specimens and the report issued in a timely manner, responsible for accuracy.
9, coordinated with the physical and chemical laboratory personnel work arrangements to ensure that the physical and chemical testing work properly.
Quality management system staff duties Part 11
1, participate in the maintenance and supervision of the quality system operation, organization and management of internal quality audits.
2, according to the operating instructions and the corresponding process of inspection of materials and spare parts, fill in the inspection records, and submit to the quality director.
3, summarize and archive the quality inspection records and related information.
4, the production process quality inspection and control, timely reporting of batch quality problems.
5, the finished product shipment inspection control, to ensure that the finished product all qualified.
6, to assist the quality supervisor to complete other quality management system aspects of the work.
Quality management system clerk's job responsibilities Part 12
1, collect the production progress of outgoing factories, order arrangements;
2, responsible for product follow-up work, supervise the production progress and quality of outgoing factories, to complete the mid-term, late quality inspection report, and supervise to ensure that it can be shipped out on schedule;
3, deal with the abnormalities that occur in the process of production or Emergencies, timely proposals to solve the problem, and submit a timely report to the superior;
4, responsible for the order production process information summary, reporting and feedback, tracking the use of materials and the number of cases;
5, have a basic level of computer operation, proficient in the use of WORD, EXCEL computer documents.
Quality management system staff duties Part 13
1, responsible for the production workshop product quality inspection work.
2, do a good job in the production stage of the intermediate inspection, fill out the intermediate inspection record ledger.
3, the size of the product on the shift, negative difference, product classification, sub-numbering and surface quality issues responsible for the overall.
4, supervise the quality inspection of each position, and coordinate the inspection of each process.
5, do a good job of waste and change the judgment and classification of products.
6, the emergence of major quality problems in a timely manner to the Department of Quality Supervision report, the implementation of the Department of Quality Supervision on the quality management of the provisions.
7, supervise the quality inspection records of the team, and be responsible for the completeness and accuracy of the data.
8, maintain good labor discipline and post balance of the team to ensure that the work is carried out properly.
9, to improve the production safety of the team.
Quality management system staff duties Part 14
1, responsible for the daily production of quality inspection.
2, responsible for raw materials, purchased parts, outsourcing processing parts of the warehouse inspection.
3, responsible for the finished product general inspection and issue a certificate of conformity.
4, the preparation of quality management system, and is responsible for the implementation; drafting quality bulletin and is responsible for the implementation.
5, proposed to convene regular or temporary quality meetings.
6, participate in the workshop process tooling preparation, evaluation of process tooling reliability.
7, coordinate with the technical department to sign the opinion on the treatment of waste and defective products.
Quality management system staff duties Part 15
1, establish the quality is the life of the enterprise, love this job, enhance the sense of responsibility.
2, proficient in finished products, semi-finished products and raw materials, grade quality standards, and dutifully complete their duties.
3, the work of tracking and inspection without error, without omission. Physical and chemical, technical and other data accurately, found that the quality of timely reporting.
4, conscientiously fulfill their duties, product quality is not qualified not packaging, not the next process, to ensure that the quality of the product before leaving the factory.
5, supervise and check the quality of each production position, guide employees to work according to operating procedures, to prevent foreign objects into the finished product, resulting in quality accidents.
6, maintenance of quality testing equipment (apparatus), seriously do a good job of quality inspection records, keep good quality file information.
7, the product is not factory, the quality of the product has the main responsibility.
Quality management system clerk job responsibilities Part 161, follow up the production progress of the big goods, do a good job of quality control, to ensure that the order is shipped on time;
2, according to the quality inspection system of the finished product shipped to the full inspection, in order to ensure the quality of clothing, such as clothing pattern, fabrics, color, threads, breakage, etc.;
3, on the quality inspection problems for the record, analyze, and Develop solutions and preventive measures;
4, quarter-end statistics of defective products, determine the cause of defective products, to ensure the reasonableness of the determination, defective products maintenance, to ensure that the quality and timeliness of repair, and make the appropriate registration
Quality Management System Staff Job Responsibilities Part 17Position Objective: To implement the Drug Administration Law and the GSP, to ensure that the quality system of the company is running normally, responsible for the company's Quality management implementation; responsible for the maintenance and quality inspection of the drugs in the warehouse; responsible for the company's purchase and sale of drugs and equipment in and out of the warehouse acceptance review, collect the quality of drugs and equipment in the warehouse related documents and scanning archives; to ensure that the company's legitimate business, quality services to meet the needs.
Job responsibilities:
1, responsible for drug quality management, effective exercise of quality supervision and management functions.
2, responsible for the development, improvement and updating of quality system documents, collection and implementation, implementation of national laws and regulations on drug management and the requirements of the notice.
3, adhere to the principle of quality, reject the unqualified drugs into the warehouse, the effective exercise of the veto power; with the "acceptance", "accompanying the goods with the single", "sales return single" in the specified time and place, according to the legal standards and quality acceptance procedures and rules of the purchased drugs, sales of returned medicines, batch by batch for acceptance.
4, is responsible for the maintenance of drugs and medical devices in storage, regular quality maintenance checks on the stock of drugs, responsible for the establishment of acceptance, maintenance information files.
5, guidance and supervision of the warehouse drugs custody, maintenance and transportation in the quality of work.
6, check the storage conditions of the drugs in the warehouse, guidance and cooperation with the custodian of the warehouse temperature, humidity management, do a good job of temperature and humidity records in the warehouse; the temperature of the emergence of anomalies to take appropriate measures.
7, regularly summarize, analyze and report the quality information of maintenance inspection, near-expiry drugs.
8, is responsible for all the company's business varieties of complete qualification documents and each batch of factory inspection reports and other information on file storage and updating work.
9, is responsible for the management of species, the first enterprise, customer information, and the purchase agreement, the purchase contract approval.
10, is responsible for the first business enterprises, supply units, purchasing units, new products, the first business information system input and its legitimacy of the audit, and the qualifications of the above monitoring, updating, to ensure that it continues to be legal and effective.
11, is responsible for the company's drugs and medical equipment procurement and sale of the return acceptance, drug test report organization and archiving.
12, is responsible for the quality of the drugs operated by the file and suppliers, customer information declaration and entry, the information change report.
13, responsible for the quality system documents, laws and regulations, and headquarters or the drug regulatory department issued a variety of documents filing and preservation.
14, is responsible for unqualified drug confirmation, summary, analysis, reporting, destruction, and supervision of the process of unqualified drugs.
15, responsible for drug quality inquiries and drug quality accidents or quality complaints of the investigation, handling reports.
16, responsible for the organization and implementation of the relevant departments of the quality of the drug recall; according to all levels of pharmacological supervision department and the higher authorities notice, responsible for the operation of the verification of drug emergencies.
17, is responsible for maintaining good communication with the pharmaceutical industry associations, drug supervision and management departments at all levels, and is responsible for the relevant departments of the company's drug and medical device business license and GSP of the external audit inspection.
18, regular internal review and inspection of the company's GSP certification system and the implementation of quality management system
19, responsible for quality management. Organization, publicity, implementation, internal inspection and feedback
20, to assist the Ministry of Human Resources to carry out education on the quality management of pharmaceuticals for employees, GSP training
21, to complete the other work assigned by the higher leadership.
Quality management system staff duties 18
1. conscientiously carry out the implementation of the Drug Administration Law and relevant laws and regulations and administrative regulations, responsible for the quality of the whole process of drug business supervision, inspection, guidance, in the enterprise on the quality of drugs with the right to rule.
2. Responsible for drafting the enterprise quality management system, and the implementation of the system to guide the supervision and inspection, and have records.
3. Responsible for investigating, handling and reporting quality inquiries, quality complaints and quality accidents.
4. Guide and supervise the quality work in the process of purchase, acceptance, maintenance and sales.
5. Regularly organize and hold enterprise quality analysis meetings, summary and timely report the situation.
6. Audit and confirmation of unqualified drugs, and the implementation of the process of handling supervision and make process records.
7. Responsible for the collection, collation, analysis and transmission of quality information, and regular statistics.
8. Responsible for the processing and reporting of adverse drug reaction information.
9. Responsible for the audit of the first enterprise and the first varieties.
10. Responsible for the establishment of the operation of the drug quality standards, including drug quality standards and other content of the quality file.
11. To assist the enterprise personnel to carry out quality education and training of employees.
Quality management system staff duties 19
1. To assume primary responsibility for the quality of drugs in the pharmacy.
2. Responsible for the daily management of the pharmacy.
3. Responsible for providing the necessary working conditions to ensure that the pharmacy quality manager to effectively fulfill their duties.
4. Should be a licensed pharmacist, and to perform the relevant duties of a licensed pharmacist, can carry out prescription review and pharmacy services.
5. Ensure that the enterprise operates drugs in accordance with the requirements of this Code.
6. Responsible for the setup of the pharmacy quality management organization, to determine the quality management functions of each post and the quality veto power of the quality manager.
7. Finalize the pharmacy quality management system.
8. Research and determine the major issues of pharmacy management.
9. Determine the quality of pharmacy staff incentives and penalties. 10. Develop and organize the implementation of the internal management structure of the pharmacy program.
11. Formulate the basic management system of the pharmacy and the formulation of specific regulations of the pharmacy and participate in the assessment of the implementation of the system.
12. Decide on the appointment or dismissal of employees, the formulation of employee wages, benefits, rewards and punishments.
13. Responsible for the internal and external environmental health of the pharmacy cleanliness checks to ensure that the pharmacy property and employee safety.
14. Responsible for the reception of foreign guests and the organization of foreign personnel to visit, study and other work.
15. Responsible for the management and deployment of office supplies, office equipment, and the receipt and distribution of documents and information, management.
16. Responsible for pharmacy license, annual inspection, replacement and other matters.
17. Responsible for the development, organization and implementation of training programs for pharmacy staff. Review and confirmation of academic and technical certificates, annual organization of staff health checks, health abnormalities, transfer out of the original position, and the establishment of training, health records.
Quality management system staff duties Part 20
1, the quality of the branch factory in charge.
2, collect, summarize and analyze the original records of quality, and promote the improvement of billet quality.
3, the occurrence of secondary and above quality accidents organization to convene an analysis, determine the relevant responsibility, put forward preventive measures and rectification programs.
4, responsible for the scene of nonconforming products, reclassification of steel responsibility determination and analysis of the causes of quality accidents, and put forward preventive and corrective measures.
5, dealing with quality objections to the complaint, timely report to the factory leadership.
6, regularly report the quality situation to the plant manager, the technical director in charge of the plant, section chiefs and sections.
7, regularly out of a variety of reports (quality monthly report, etc.).
8, to determine the responsibility for the rolled steel scrap, and is responsible for the user's quality objections to the claim processing.
9, the development of annual quality policy, target assessment methods and is responsible for checking the implementation of the completion of the situation.
10, participate in the company, the plant organization of quality research work.
11, monthly on time to provide quality assessment based on the integrated section.
12, do a good job in the day-to-day management of the standard.
13, on time to organize the monthly internal standard simulation of internal audit
14, responsible for liaison with higher quality departments.
15, participate in the organization of the reception of the company's annual internal audit of the standard and the National Quality Certification Center of the external audit.
16, responsible for the management of documents and information archives.
17, responsible for quality records of the inspection, assessment.
18, the organization of coherent standard document revision.
19, according to the requirements of the completion of the factory, the section under the temporary work.
Functional authority:
1. Responsible for the preparation of the department's management system, to assist in the preparation of inspection procedures;
2. To assist the manager of the quality department to organize the preparation of the company's quality management system documents;
3. Specifically responsible for the quality of statistical analysis of data;
4. p>
4. Responsible for the collection of quality records and archiving management
Terms and Conditions:
1. With college education or above;
2. With medical related majors;
3. Familiar with the medical device related laws, regulations and standards;
4. Familiar with the production process, inspection norms and medical device products. Familiar with the production process of medical devices, test specifications and related standards;
5. More than two years of experience in quality management, quality management and internal audit experience;
;