1. Responsible for quality supervision of each batch of drug production and inspection process; communicate with CMO in time for tracking and rectification of problems found during inspection; 2. Participate in dealing with deviations, changes, returns, etc. during the production process; 3. Audit product process protocols, batch production records (blank), process/cleaning validation programs and reports; 4. Audit batch production records, batch inspection records, complete product release audit, batch file archiving; 5. Participate in CMO, material supplier site quality audit; 6. Draft quality agreements for commissioned production of pharmaceutical products, check the design of printed packaging materials and other text content information; 7. Responsible for product annual quality review report data collection and audit; 8. Participate in the collection and audit of B license additions; participate in GMP compliance checks. Qualifications 1. Bachelor degree or above in pharmacy related majors; 2. 2 years and above working experience in sterile preparation, engaged in QA or production management related work; 3. Familiar with drug administration law, drug production supervision and management methods, GMP, MAH related laws and regulations; 4. Adapt to business trip, work conscientiously and responsibly, and be good at communication with the outside.

1. According to the approved process protocols and batch record templates provided by the entrusted party, draft and audit the process protocols and batch records of our products under development and/or held products, and revise them in due course according to the actual situation. 2. Audit and sign the batch records of completed products in accordance with the provisions of “Drug Listing and Release Management Procedures”. Collect, summarize and analyze the key process parameters of the listed products to provide information for technical improvement and process optimization. 3. Participate in the audit of commissioned drug manufacturers, assess the production conditions of commissioned drug manufacturers such as plant facilities and equipment. 4. Participate in the audit of the research product pilot release of large quantities, registration and declaration of batch production programs and reports and other technical documents. 5. Participate in the supervision and guidance of the commissioned production process, supervise and guide the commissioned party to produce qualified products in accordance with the approved production process. 6. Participate in the entrusted party in the commissioned drug research and development, production process of all kinds of abnormalities, production accidents, quality accidents in the investigation and treatment, collect/analyze the product process technology problems and hidden trouble points, develop preventive measures and supervise the implementation. Qualifications 1. Bachelor degree or above in pharmacy or related majors or university college has engaged in pharmaceutical production, quality practice and management for more than 3 years of experience. 2. Familiar with GMP, familiar with the pharmaceutical industry related national policies, laws and regulations, familiar with drug production management. 3. Have good team management ability, organization ability, communication and coordination ability, overall planning ability, execution ability.

1. Responsible for national market development, marketing / product / price / channel management and other work, organize to establish and improve the marketing network; 2. Responsible for the development and volume of the company's products, manage regional agent to ensure the realization of sales targets; 3. Responsible for the national market research, including demand analysis, customer analysis, competitor research and policy research, etc., to provide support data for the company's decision-making; Qualifications: 1. Bachelor degree or above; 2. More than 5-10 years of experience in pharmaceutical, biotechnology industry or pharmaceutical outsourcing companies and other specialized companies; 3. Successful experience of working in pharmaceutical omni-channel especially in the retail side.

1. Responsible for the company's marketing department and drug strategy research; 2. Responsible for national policy research; 3. Responsible for market information collection, collation, research; 4. Develop the company's drug market strategy combined with the company's development strategy; 5. Responsible for new product listing promotion planning. Qualifications: 1. Bachelor degree or above; 2. More than 5-10 years of experience in pharmaceutical, biotechnology industry or pharmaceutical outsourcing companies and other specialized companies; 3. Successful experience in drug strategy development in ophthalmology or ENT medicine and head of marketing.