1. Master's degree or above, with a background in clinical medicine and at least 3 years of work experience. Candidates with experience as a psychiatrist are preferred;
2. Familiar with the diagnosis and treatment process of common clinical diseases, with a deep understanding and insight into disease diagnosis and treatment, experience in mental disorders is preferred;
3. Strong medical writing ability, proficient in domestic and foreign medical and pharmaceutical literature retrieval;
4. Strong English reading and translation skills, supporting domestic and international project meetings and literature translation work;
5. Strong communication skills, language expression ability, and cross departmental collaboration ability;
6. Familiar with the requirements of ICH-GCP, drug development process, and relevant registration regulations.
1. Complete the writing or review of clinical trial protocols, informed consent forms, investigator manuals, and other materials;
2. Participate in the selection process of clinical research centers and major researchers, visit researchers from various centers, communicate important medical matters related to projects with researchers, participate in protocol discussion meetings, support ethics review meetings and center kickoff meetings;
3. Conduct medical monitoring of ongoing projects, including reviewing subject eligibility for enrollment, reviewing AE/SAE reports, developing PD listings and regular maintenance, reviewing PD reported by the center, conducting medical reviews of EDC or research center data, raising medical questions, and following up on response to questions;
4. Cooperate with the clinical department to promote clinical research and provide medical training to CRA, CRC, and other clinical research participants;
5. Review clinical trial summary reports and other application materials (medical section);
6. Conduct research on the drugs currently under development or planned for development by the company (including clinical applications and current research status of similar drugs), and summarize and analyze relevant literature or data.
1. Education and major requirements: Master's degree or above, major in pharmacy or chemistry related fields
2. Work experience requirements: More than 6 years of work experience, and more than 4 years of drug development experience
3. Professional knowledge and job skills requirements: proficient in pharmacy, chemistry and other professional knowledge; Have knowledge in enterprise management and team management. Proficient in using computers and network resources; Proficient in translating and writing English professional literature and reports; Proficient in various professional technical operations; Proficient in using various tools related to product development and project operations; Familiar with project management knowledge, etc
4. Competency requirements: communication skills, computer application skills, planning and execution skills, innovation and learning skills, problem-solving skills, and job skills. Achievement orientation, initiative, resilience, integrity, confidentiality awareness, sense of responsibility, team spirit, discipline, loyalty, and global awareness.
1. Product research
Responsible for collecting product technical information and product technical trends;
Assist department managers in formulating the company's product and technology development strategies, and be responsible for conducting technical feasibility studies.
2. Formulation research and development
Responsible for conducting research on new products and drafting art design reports;
Responsible for organizing R&D personnel to participate in technical breakthroughs and solve technical problems;
Participate in the formulation and improvement of technical regulations and standards for company products;
Responsible for reviewing the research content of product registration materials;
Participate in the technical review of imported products and technologies, formulate digestion and absorption measures, and organize their implementation;
Assist in the review of corresponding module product research cases, research plans, experimental records, research reports, and registration materials;
Complete the standards for managing equipment, including SOP, maintenance, upkeep, repair reporting, calibration, and other related records.
3. Technical Management
Assist in formulating the technology development plan for the R&D module and regularly report on the progress of technology development;
Assist in formulating intellectual property development plans for the module and regularly report on technological progress;
Improve the research and development technology platform and database;
Assist in improving production technology and tackling key projects, and evaluate the results of the projects;
Provide guidance on new product art and assist downstream departments in achieving large-scale production;
Professional technical training (including research and development technology, art technology, etc.) and talent training;
Assist department managers in organizing the introduction, development, and implementation of new technologies and techniques;
Responsible for the formulation research of project teams that require technical breakthroughs.
1. Bachelor's degree or above in finance, accounting, economics or related majors, holding an accounting professional qualification certificate, and having a junior professional title is preferred;
2. More than two years of experience in cashier and finance work, with priority given to those with work experience in pharmaceutical manufacturing enterprises;
3. Proficient in using office software such as Word and Excel, with experience in using financial software such as T6, UFIDA, Kingdee, etc;
4. Work meticulously and meticulously, with clear thinking and a strong sense of responsibility, possessing excellent communication skills and teamwork spirit.
1. Responsible for the daily receipt and payment, inventory and verification of cash and bank deposits in the company, ensuring that accounts match;
2. Proficient in operating enterprise online banking, handling various daily transactions such as transfers, payments, remittances, and receipt inquiries;
3. Responsible for handling relevant procedures such as opening, changing, and closing company bank accounts;
4. Timely register cash journal and bank deposit journal to achieve daily clearing and monthly settlement;
5. Responsible for registering electronic contract ledger and organizing scanned copies of electronic contracts;
6. Assist superiors in coordinating bank credit work;
7. Assist in voucher binding, asset inventory, and other related tasks;
8. Complete other financial related tasks assigned by superiors according to company needs.
1. College degree or above, majoring in pharmacy or related fields.
2. Having over 1 year of experience in laboratory physical and chemical testing.
3. Master conventional physical and chemical analysis techniques, familiar with experimental principles and instrument skills;
4. Proficient in using, maintaining, and calibrating various physical and chemical testing instruments, such as UV spectrophotometers, infrared spectrometers, TOC analyzers, etc; Capable of data processing and analysis.
5. Seek truth from facts and be honest and upright, objective and fair, faithful to the original data, never tamper with or fabricate data; Strong analytical ability, able to comprehensively analyze multiple detection indicators to make reasonable explanations and preliminary judgments on the results.
1. Responsible for inspecting the physical and chemical analysis items of intermediate products and finished product samples produced by the company;
2. Responsible for sampling and inspecting raw materials and packaging materials;
3. Responsible for inspecting the stability of the products produced and testing the samples;
4. Responsible for sampling and inspecting the production process/steam;
5. Responsible for the management of chemical reagents, samples, and reference materials in the QC department;
6. Responsible for the regular maintenance, upkeep, and declaration of repairs of laboratory instruments and equipment;
7. Responsible for drafting product quality standards and physical and chemical testing SOPs;
8. Responsible for handling and investigating anomalies/deviations, OOS/OOT during the inspection process, and developing corresponding preventive measures.
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