In life, we are all directly or indirectly related to job responsibilities. We can make clear what everyone's job responsibilities are, what kind of work they should undertake, what kind of responsibilities they should undertake, how to do better, what they should not do, and so on. What kind of job responsibilities are effective? The following are the job responsibilities (5 selected articles) of the quality controller I collected, hoping to help you.
Job responsibilities of quality controller 1 job description:
1, material release;
2. Deviation investigation;
3. Perform daily GMP inspection to ensure that all operations are carried out in strict accordance with SOP;
4. Implement supplier quality system management and organize supplier evaluation and audit;
5. Draft annual quality management plans and reports, calibration plans and reports;
6. Review and update the management scope of SOP;
7, responsible for the management within the scope of the test.
Requirements:
1 year above QC experiment experience in GMP pharmaceutical factory or 2 years above QA experience in quality assurance department;
Familiar with relevant requirements of cGMP (CFDA, etc.). );
3. Those who have participated in FDA or GMP certification are preferred, and those with internal auditor qualification or supplier management experience are preferred;
4. Have a strong sense of responsibility and learning ability, and good expression and communication skills; Willing to accept challenges, with good professional ethics, professionalism and teamwork spirit.
Responsibility of QC 2 1, responsible for the system audit of the first camp enterprises and the first camp varieties, and keeping the data number on file.
2, responsible for the special drug sales system audit.
3, responsible for suppliers, sales customers, varieties and other recent data system updates, and archiving.
4, responsible for the system audit of unqualified drugs, and supervise the destruction of unqualified drugs.
5. Responsible for the distribution and recycling of documents.
6, responsible for drug quality query, and keep records.
7, responsible for maintenance personnel, keeper, etc. Guide the daily work and keep records.
8, responsible for the collection and transmission of drug information, and make records.
9. Assist the director of quality control department to carry out other work.
Job responsibilities of quality controller 3 I. Organizational structure:
The quality supervision team is directly led by the department director, and the team leader organizes the activities of the facility group. The team members are composed of professional and technical personnel recommended by the leaders of each working group as needed.
Team leader: Cai Changlin
Deputy team leaders: Wen and Zheng
Members: Ling, Li, Chi Huanjiao
Second, the job responsibilities:
1. The quality supervision and management team supervises, feeds back, analyzes and summarizes the drug quality management and processes of various departments in the pharmacy department according to the Drug Administration Law, GSP Drug Management Standards and Prescription Management Measures.
2, implement the management rules and regulations of the department, objectively and fairly evaluate the implementation of the quality management system, improve the level of drug quality management;
3. Supervise the implementation of pharmacists and responsible pharmacists at all levels in their respective posts and the implementation of rules and regulations.
4, timely analysis and rectification department leaders feedback drug quality management problems, improve the level of pharmaceutical quality management.
Job responsibilities of quality controller 4 1. Responsible for collecting laws, regulations and other relevant provisions related to medical device management and implementing dynamic management;
2. Supervise relevant departments and post personnel to implement medical device laws and regulations and this specification;
3. Responsible for the qualification examination of medical device suppliers, products and buyers;
4. Responsible for the confirmation of unqualified medical devices, and supervise the handling process of unqualified medical devices;
5 responsible for the investigation, handling and reporting of medical device quality complaints and quality accidents;
6. Organize the verification and calibration of relevant facilities and equipment;
7. Organize the collection and reporting of medical device adverse events;
8. Responsible for the management of medical device recall;
9. Organize the review of the transportation conditions and quality assurance ability of the entrusted transportation carrier;
10. Organize or assist in quality management training;
1 1. Other duties that should be performed by quality management organizations or quality management personnel.
Qualifications:
1. Major related to medical devices (medical devices, biomedical engineering, medicine, bioengineering, chemistry, pharmacy, etc. ) with college degree or above or intermediate title.
2. Have more than 3 years working experience in quality management of medical devices.
3. Have team spirit.
Responsibilities of quality administrator 5 1. Supervise relevant personnel to implement drug management laws and regulations, GSP and related quality management system.
2, conscientiously implement the quality policy of pharmacy, guide and supervise the implementation of pharmacy related quality management documents.
3, responsible for drug acceptance, guidance and supervision of drug display, sales and other aspects of quality management.
4, responsible for drug quality query and quality information management.
5, responsible for the investigation, handling and reporting of drug quality complaints and quality accidents.
6, responsible for the unqualified drugs according to the pharmacy unqualified drug management system to confirm and deal with.
7, responsible for reporting counterfeit drugs to the local drug regulatory authorities.
8. Be responsible for adverse drug reactions in accordance with the Management System of Adverse Drug Reaction Reports in Pharmacy.
9, to assist the headquarters to carry out drug quality management education and training.
10, responsible for organizing the calibration and verification of measuring instruments.
1 1, to guide and supervise pharmaceutical services.
12. Strengthen the management of drug expiration date and set up the "Report Form for Prompt Sales of Expired Drugs". According to the principle of "first production, first change, first change, first out, first near, then far away", a report form should be filled out once a month when the drug is six months away from its expiration date.
13. Implement the Drug Administration Law and GSP, and be responsible for the quality supervision of the whole process of drugs.
14, the final treatment of drug management quality problems.
15, responsible for the formulation, revision and review of quality management documents.
16. Be responsible for organizing and implementing the audit of GSP on a regular basis, and report the inspection results to the person in charge in writing in time, and put forward improvement measures.
17, responsible for organizing users to pay a return visit, and having the right to decide and handle users' opinions, return goods and unqualified drugs.
18, responsible for supervising and inspecting the implementation of quality management.
19. Other duties that should be performed by quality management personnel.
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