Responsibilities of quality director 1
? Organize the revision, distribution and implementation of the company's quality management system documents;
? Organize the publicity and training of knowledge related to the implementation of quality management system;
? Organize and implement the training of internal auditors of the company's quality management system;
? Responsible for the collection, publicity and training of national and local laws and regulations on quality;
? Participate in the acceptance of branch projects (basic branch projects and main branch projects) and completed projects;
? Participate in the service work of completed projects;
? Organize engineering quality inspection and review of rectification effect;
? Participate in the investigation, report, analysis and handling of quality accidents;
? Organize the implementation of the company's project quality excellence plan;
? Participate in promoting QC group activities;
? Responsible for project return visit and customer satisfaction survey;
? Responsible for engineering warranty management;
? Lead other work temporarily assigned.
Responsibilities of Quality Director 2
1. Take charge of the work of this department, be responsible for the overall work of the quality management department, ensure that the company's drug production meets GMP requirements, and put forward opinions and improvement suggestions to the company leaders in time to ensure product quality.
2. Fully responsible for the internal management of the department, including safety, assessment, staff training, plan summary, rules and regulations construction, etc.
3. Formulate internal control quality standards for enterprises and organize GMP self-inspection regularly.
4. Deal with the product quality problems reflected by users, and organize relevant departments to study the improvement measures of quality problems.
5. Participate in the pilot test, trial production and on-site inspection of the company's new products.
Responsibilities of Quality Director 3
1, standard specification for quality system of residential quarters in management company;
2. Formulate the company's quality control workflow and operation specifications; Formulate the quality objectives and quality work plans of the enterprise;
3, organize the implementation of quality control workflow specification and quality work plan, and supervise the implementation;
4. Coordinate and communicate with relevant departments inside and outside the enterprise, and actively organize quality management;
5. Supervise and guide the quality control in the production process of enterprises, and establish a quality supervision and feedback mechanism;
6. Be responsible for handling quality disputes of enterprises and analyzing major quality accidents;
7. Discuss with the production department and relevant departments and put forward quality improvement measures;
8, responsible for guiding the daily work of the quality department, and training and assessment of subordinates.
9. Fully responsible for the authoritative quality certification in the country and around the world.
Responsibilities of Quality Director 4
1, guide enterprises to establish and implement various management systems (national military standard GJB900 1, military support system, scientific research and production license of weapons and equipment, equipment qualification review, ISO900 1, ISO 1400 1, OHSAS1.
2 to guide enterprises to establish rules and regulations should be combined with the actual situation of enterprises, improve the management level of enterprises.
Qualifications:
1, college degree or above, proficient in computer application and rich experience in enterprise consulting.
2, aged between 28-55 years old, healthy, handsome, accurate and vivid language expression; Modesty and team spirit.
3. Those with national registered auditor or consultant qualification certificate are preferred.
4. Have a military background and be familiar with the requirements of military four certificates is preferred.
5, familiar with the standard process, accurate audit standards, vivid and accurate lectures, patient and meticulous guidance, to achieve customer satisfaction.
Responsibilities of Quality Director 5
1, belonging to the company's middle and senior management positions, in charge of quality, regulations, document control and other work. Implement the laws and regulations on medical device quality management, lead the overall planning and construction of the company's quality management system, and do a good job in communication and coordination with relevant government departments;
2. Strictly implement the production quality management system to ensure product quality, including but not limited to: approval of system documents; Process verification and approval of key processes; Approve the quality control standards for raw materials, semi-finished products and finished products; Selection of suppliers of key raw materials; Selection of key production and test equipment, etc.
3. Be responsible for the registration of medical regulations and products, track the trends of CFDA's laws and regulations, organize the collection and arrangement of registration regulations, coordinate the required resources according to the company's strategic objectives, formulate the company's product registration plan, and organize registration (domestic and international);
4. Maintain interaction with regulatory agencies, keep abreast of changes in policies and regulations, take the lead in organizing internal audit and risk assessment of the quality system, and regularly organize evaluation of the operation of the quality management system to ensure effective quality control in all aspects of product production;
Responsibilities of Quality Director 6
1. Establish the quality target system of the company and business departments, and cooperate with the enterprise management department for tracking and assessment;
2. Establish a quality target data management system to collect, summarize and analyze relevant quality data; Be responsible for analyzing quality problems, proposing quality improvement suggestions, organizing quality meetings and implementing rectification;
3. Be responsible for handling the company's quality accidents (poor design, poor batch technology, poor parts). Organize the investigation, analysis and coordination of various quality anomalies, and provide technical support for quality problems in the production process;
4. Be responsible for the establishment and continuous improvement of quality assurance systems such as incoming inspection, process quality control and ex-factory quality control in the plate, as well as the construction of supplier quality management system and on-site quality monitoring system;
5. Be responsible for the quality education of all employees, publicize and establish a good corporate culture for all employees to participate in quality management and supervision;
6. Be responsible for promoting the effective operation and continuous improvement of the company's quality system, occupational health and environment system.
Responsibilities of Quality Director 7
1, fully responsible for the company's quality system management;
2. Be responsible for establishing, implementing and maintaining the effective operation of the company's quality system: organize the formulation of the company's quality policy, the establishment, implementation and guarantee of the quality management system and corresponding quality indicators, establish and continuously improve the company's quality management system, and realize the continuous improvement of quality management.
3. Be responsible for establishing laboratory and factory quality control according to GMP requirements to ensure the controllable project quality;
4. Responsible for on-site quality control;
5, responsible for maintaining communication and exchanges with the drug administration department, timely convey the relevant laws and policies of the national drug administration;
6. Quality compliance management of new drug research and development;
7. Responsible for internal/external audit to ensure that the internal system of the company meets the audit requirements and the selection of external suppliers meets the SOP requirements;
8. Responsible for updating, maintaining and establishing sop, which may involve clinical operation, medical writing and planning, pharmacovigilance and supplier evaluation;
9. Participate in major technical activities such as enterprise technological transformation, new product research and development, and technical research.
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