Job Responsibilities:
1. Collecting and analyzing drug quality information, supervising and guiding the quality management of drugs in the processes of procurement, acceptance, storage, maintenance, and sales;
2. Responsible for handling drug quality inquiries, consultations, and the investigation, handling, and reporting of quality incidents or complaints; reviewing and supervising the disposal of unqualified drugs before they are written off and ensuring proper records are kept for unqualified drugs;
3. Responsible for establishing quality files for the drugs sold in the store, including quality standards, and assisting the Quality Management Department in implementing (GSP) management and supervising its implementation;
4. Responsible for daily cashiering work in the store, filling in basic cashier forms as required by the company;
5. Adhering to company rules and regulations, and completing other tasks assigned by superiors.
Job Requirements:
1. College degree or above, with a background in medicine, pharmacy, nursing, or other related fields, and a licensed pharmacist title is preferred;
2. Proficient in using office software such as Excel, Word, etc.;
3. Hardworking, meticulous, and responsible with a strong sense of work responsibility.
Job Responsibilities:
1. Participate in audits of entrusted enterprises and suppliers, and track the rectification status of production enterprises.
2. Draft/review risk assessment reports for co-line production quality and quality agreements for entrusted production/inspection.
3. Supervise the hygiene of entrusted production enterprises' workshops and personnel, monitor the maintenance and upkeep of factories, shared systems, and equipment, supervise GMP compliance in production and inspection processes, and review batch records.
4. Ensure completion of process validation, cleaning validation, analytical method validation, and stability studies for entrusted production products, and review related plans and reports.
5. Collect product quality review information and related data from annual reports and submit them to the QA supervisor.
6. Participate in the release review of materials, intermediate products, finished products, and production auxiliary materials for entrusted production, review non-conforming products, and supervise the handling of non-conforming products.
7. Responsible for discovering and reporting deviations, OOS/OOT during the entrusted production process, organizing deviation investigations, participating in change assessments and reviews of entrusted enterprises, organizing change implementations, identifying and describing CAPA non-conformities, conducting CAPA investigations, implementing CAPA, and managing production risks.
8. Collect and organize documents and records related to production processes, quality standards, inspection methods, as well as changes, complaints, returns, recalls, confirmations/validations, and quality incidents, and ensure timely archiving.
9. Participate in product quality analysis meetings and prepare relevant materials.
Job Requirements:
1. College diploma or above in Traditional Chinese Medicine or related fields;
2. At least one year of work experience in a similar position;
3. Familiar with the production process of Traditional Chinese Medicine solid dosage forms, capable of effectively monitoring key operations on-site during production;
4. Experience working as a process technician in a Traditional Chinese Medicine workshop and experience in on-site monitoring of entrusted production are preferred.
Job Responsibilities:
1. Responsible for the management of the ERP system database, data backup, and data security management. Backup data should be stored on hard drives to ensure network and data security.
2. Responsible for training and guiding relevant personnel in the use and operation of the system.
3. Responsible for the operation and maintenance management of the ERP system programs.
4. Responsible for the security management of the ERP system network and data.
5. Regularly check the usage of various devices, identify any potential security risks, and resolve any issues promptly.
6. Assign user operation permissions according to the instructions of the Quality Management Department.
7. Responsible for uploading the drug circulation supervision code to the Beijing Drug Administration.
8. Ensure the integrity of system logs.
9. Responsible for establishing management files for system hardware and software.
10. Maintain and use software and hardware.
11. Proficient in the use of office software.
