Please provide detailed explanations from experienced people about the specific work content of QA and QC positions in pharmaceutical companies. Thanks!

The specific content of QC job positions in pharmaceutical companies: Responsible for the quality inspection (physical and chemical inspection and microbial inspection) of process water, raw materials, finished products, semi-finished products, and packaging materials; responsible for the reagent cabinets and analytical pure reagents, inspection materials Management of drugs, responsible for verification of testing methods for various varieties, and maintenance of experimental equipment.

The specific contents of QA job positions in pharmaceutical companies: Responsible for quality control of the workshop product manufacturing process, sampling of semi-finished products, products to be packaged, and finished products and their release to the next process, supervising and inspecting the on-site inventory process of the production workshop, and monitoring packaging process. Responsible for the inspection of semi-finished products particles, weight difference items and appearance inspection of each process of the product, filling in the semi-finished product transfer card, responsible for issuing process certificates and clearance certificates, responsible for retaining samples of finished products, and supervising sample sampling in the warehouse.

For fresh graduates, the salaries of QA and QC are similar. To put it simply, QC is mainly responsible for the inspection of various raw materials, finished products, semi-finished products, process water and other physical and chemical items and microbiological items. QA is mainly responsible for the production site, monitoring the entire process of producing drugs, and is responsible for retaining and sending batch samples for inspection (to QC).

Extended information:

QA verification work content: Develop an enterprise verification plan, establish a verification team based on the objects to be verified, propose verification projects, formulate verification plans, and organize implementation. Coordinate and drive analysis during the validation process and complete validation reports upon completion of validation. After a certain period of production, the management will be verified. Responsible for validating reviews and recommendations. The data and analysis content during the summary and verification process are archived and saved in the form of files.

Fresh graduates are generally only responsible for on-site monitoring in QA, while verification work requires accumulation of a lot of work experience and has higher requirements. If you want to learn about drug production management, it is recommended to go to QA, and to learn various inspection methods, go to QC. Because QA is responsible for management content, it has a high online presence.

Baidu Encyclopedia——QC? Baidu Encyclopedia——QA