Drug inspector personal work summary
Time flies so fast, I have been in the company for three months. Under the guidance of the leaders, with the help of my colleagues, I insisted on learning theoretical knowledge and familiar with all the files of gmp. Through continuous practice and continuous work experience, I took over the job in just one week. So far, I have been on the post for about three months. During these three months, I strictly abide by the rules and regulations and complete the duties of my position in strict accordance with the requirements of gmp. At this juncture, I will summarize my thoughts and work as follows:
First, strengthen ideological and moral construction and continuously improve one's professional ethics.
As a party member, I always measure and demand my words and deeds by the standards of party members, pay attention to strengthening political cultivation, strengthen ideological and moral construction, and further improve my party spirit. To the party's policy, to protect the party's secrets, to comply with the company's rules and regulations, to strictly protect the company's confidentiality, in strict accordance with the requirements of gmp to complete the work, strictly abide by the test results, to achieve accurate, timely and effective data. In the work, I unite my colleagues, coordinate the handling of the relationship between colleagues and colleagues, colleagues and work, through continuous strict requirements to improve their own thinking and professional ethics.
Second, in strict accordance with the gmp regulations, sampling is representative and accurate, and the samples are not contaminated.
In the eyes of many people, sampling is a trivial matter. It can be different for pharmaceutical production companies. There are regulations on how to take samples. Disinfect measures should be taken before sampling, and self-protection measures should be taken. For example, when going to the workshop for sampling, you should wear protective clothes, hands should be disinfected with alcohol, sampling instruments should be disinfected, etc. When sampling in the warehouse, you must take samples. Sampling in the car and so on.
Third, in strict accordance with the gmp regulations, the production environment, production water testing.
Pharmaceutical production differs from other production-oriented enterprises in that it requires very strict production environments and production water.
For the production environment: the wind speed, air volume, dust particles, sedimentation bacteria, and compressed air of each production room should be tested. The continuous production is tested every six months. If the production is stopped for 15 days, all the indicators of the environment must be re-tested. The workshop environment has been tested twice and the compressed air has been tested 3 times.
For production water, all exports of production water are tested every 21 days, and three points of the pure water station are tested every day. Test items: 14 physical and chemical indicators such as traits, acidity, sulfate, calcium salt, chloride ion, nitrate, carbon dioxide, ammonia, non-volatiles, and electrical conductivity. So far, the water at the pure water station has been detected more than 60 times, and all points have been tested 4 times.
Fourth, in strict accordance with the gmp regulations, for the original auxiliary materials, the packaging materials into the factory to get off.
The production of medicines is inseparable from the original auxiliary materials and inseparable from the packaging materials. After the inspection, the corresponding original inspection records and inspection reports shall be issued. Up to now, 40 batches of raw materials and packaging materials have been tested, and 2 batches of unqualified products have been found.
5. Strictly follow the gmp regulations, do a good job in the inspection of the workshop products, so as not to delay production, without delaying the factory time.
There are 5 kinds of products produced by the company for a long time, and each product has intermediates, semi-finished products and finished products. And I have to go through the sampling and testing in every process to do quality control. After each sampling, I have to make the results in time to avoid mistakes in the production of the workshop. After the product comes out, do a full inspection of the drug, so as not to mistake the time of the product. Up to now, more than 40 intermediates and semi-finished products have been tested, and 13 batches of finished products have been tested.
Sixth, in strict accordance with the gmp regulations, fill in the use of the instrument records, do the instrument maintenance and fill in the records.
In the gmp regulations, the instrument's usage record is very important. It can detect the product you are doing in a certain period of time. It is the certificate of product inspection, and the maintenance of the instrument is more important. The instrument is easy to use. The accuracy of the instrument is inseparable from the maintenance, maintenance and self-calibration of the instrument. The use of the instrument is what is done at that time. For the maintenance and maintenance of the instrument, it is once a month. After each maintenance calibration, fill in the corresponding records.
Seven, in strict accordance with the gmp regulations, do a good job in the stability of the drug investigation, long-term inspection, and do a good job of investigation records, so far has examined more than 10 samples.
8. Strictly follow the gmp regulations, manage the highly toxic drugs, and fill in the records of the use of highly toxic drugs.
Nine, in strict accordance with the gmp regulations, the management of solid drugs, and register the use of ledgers.
X. Strictly follow the gmp regulations, manage the reference products, and use the account number for the registration number.
11. Issue inspection reports for all types of inspection products, and archive and manage the original inspection records of various types.
I have done a lot of work in this position, but no matter what I do, I treat my work with full enthusiasm, diligent, conscientious, and steadfast to complete my own work. The work in this position is complicated and there are many leaders who work in an interim manner. These require employees to have strong adaptability and adaptability. Through the work experience in the past two years, I have a comprehensive understanding and mastery of all the business work of this position! I think this aspect is the accumulation of my work. What's more important is that I have such a job opportunity in such a job. It is the result of trust and support from leaders and colleagues! For this reason, I will cherish my position more, and strive for greater progress with unparalleled enthusiasm and hard work!
In short, I have gained a lot in this position and learned a lot. This is inseparable from the support of leaders and colleagues. I know that I still have shortcomings, things are complicated, and some detailed processes are not taken into consideration in the future. In my work, I will carry forward my own strengths, make up for my shortcomings, and do my job better.
First, strengthen ideological and moral construction and continuously improve one's professional ethics.
As a party member, I always measure and demand my words and deeds by the standards of party members, pay attention to strengthening political cultivation, strengthen ideological and moral construction, and further improve my party spirit. To the party's policy, to protect the party's secrets, to comply with the company's rules and regulations, to strictly protect the company's confidentiality, in strict accordance with the requirements of gmp to complete the work, strictly abide by the test results, to achieve accurate, timely and effective data. In the work, I unite my colleagues, coordinate the handling of the relationship between colleagues and colleagues, colleagues and work, through continuous strict requirements to improve their own thinking and professional ethics.
Second, in strict accordance with the gmp regulations, sampling is representative and accurate, and the samples are not contaminated.
In the eyes of many people, sampling is a trivial matter. It can be different for pharmaceutical production companies. There are regulations on how to take samples. Disinfect measures should be taken before sampling, and self-protection measures should be taken. For example, when going to the workshop for sampling, you should wear protective clothes, hands should be disinfected with alcohol, sampling instruments should be disinfected, etc. When sampling in the warehouse, you must take samples. Sampling in the car and so on.
Third, in strict accordance with the gmp regulations, the production environment, production water testing.
Pharmaceutical production differs from other production-oriented enterprises in that it requires very strict production environments and production water.
For the production environment: the wind speed, air volume, dust particles, sedimentation bacteria, and compressed air of each production room should be tested. The continuous production is tested every six months. If the production is stopped for 15 days, all the indicators of the environment must be re-tested. The workshop environment has been tested twice and the compressed air has been tested 3 times.
For production water, all exports of production water are tested every 21 days, and three points of the pure water station are tested every day. Test items: 14 physical and chemical indicators such as traits, acidity, sulfate, calcium salt, chloride ion, nitrate, carbon dioxide, ammonia, non-volatiles, and electrical conductivity. So far, the water at the pure water station has been detected more than 60 times, and all points have been tested 4 times.
Fourth, in strict accordance with the gmp regulations, for the original auxiliary materials, the packaging materials into the factory to get off.
The production of medicines is inseparable from the original auxiliary materials and inseparable from the packaging materials. After the inspection, the corresponding original inspection records and inspection reports shall be issued. Up to now, 40 batches of raw materials and packaging materials have been tested, and 2 batches of unqualified products have been found.
5. Strictly follow the gmp regulations, do a good job in the inspection of the workshop products, so as not to delay production, without delaying the factory time.
There are 5 kinds of products produced by the company for a long time, and each product has intermediates, semi-finished products and finished products. And I have to go through the sampling and testing in every process to do quality control. After each sampling, I have to make the results in time to avoid mistakes in the production of the workshop. After the product comes out, do a full inspection of the drug, so as not to mistake the time of the product. Up to now, more than 40 intermediates and semi-finished products have been tested, and 13 batches of finished products have been tested.
Sixth, in strict accordance with the gmp regulations, fill in the use of the instrument records, do the instrument maintenance and fill in the records.
In the gmp regulations, the instrument's usage record is very important. It can detect the product you are doing in a certain period of time. It is the certificate of product inspection, and the maintenance of the instrument is more important. The instrument is easy to use. The accuracy of the instrument is inseparable from the maintenance, maintenance and self-calibration of the instrument. The use of the instrument is what is done at that time. For the maintenance and maintenance of the instrument, it is once a month. After each maintenance calibration, fill in the corresponding records.
Seven, in strict accordance with the gmp regulations, do a good job in the stability of the drug investigation, long-term inspection, and do a good job of investigation records, so far has examined more than 10 samples.
8. Strictly follow the gmp regulations, manage the highly toxic drugs, and fill in the records of the use of highly toxic drugs.
Nine, in strict accordance with the gmp regulations, the management of solid drugs, and register the use of ledgers.
X. Strictly follow the gmp regulations, manage the reference products, and use the account number for the registration number.
11. Issue inspection reports for all types of inspection products, and archive and manage the original inspection records of various types.
I have done a lot of work in this position, but no matter what I do, I treat my work with full enthusiasm, diligent, conscientious, and steadfast to complete my own work. The work in this position is complicated and there are many leaders who work in an interim manner. These require employees to have strong adaptability and adaptability. Through the work experience in the past two years, I have a comprehensive understanding and mastery of all the business work of this position! I think this aspect is the accumulation of my work. What's more important is that I have such a job opportunity in such a job. It is the result of trust and support from leaders and colleagues! For this reason, I will cherish my position more, and strive for greater progress with unparalleled enthusiasm and hard work!
In short, I have gained a lot in this position and learned a lot. This is inseparable from the support of leaders and colleagues. I know that I still have shortcomings, things are complicated, and some detailed processes are not taken into consideration in the future. In my work, I will carry forward my own strengths, make up for my shortcomings, and do my job better.
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