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Job Responsibilities:

1. Apply expertise in molecular biology theories and techniques to support the advancement of drug R&D projects.

2. Elucidate mechanisms of drug targets through experimental design.

3. Conduct molecular cloning, gene expression analysis, protein purification, and characterization.

4. Collaborate with cross-functional teams to develop and optimize high-throughput screening methods for drug molecules.

5. Analyze complex biological data and contribute to data-driven decision making.

6. Stay abreast of the latest scientific developments and propose innovative strategies.

Job requirements:

1. Ph.D. in Molecular Biology, Biochemistry, or related field; more than 3 years of relevant work experience.

2. Strong professional background in molecular biology techniques, including gene expression analysis, cloning, and protein characterization.

3. Proficiency in using advanced biological laboratory instruments and molecular biology software.

4. Ability to independently design and conduct experiments.

5. Strong scientific thinking ability, with skills in problem analysis and problem solving.

6. Excellent communication skills and ability to collaborate effectively in multidisciplinary teams.

7. Prior experience in new drug R&D is preferred.

Responsibilities:

1. Participate in developing medical strategies across the full product lifecycle, including clinical trial design, indication expansion, and post-marketing medical plans.

2. Provide clinical research support, assist in conducting clinical trials, and review study protocols, investigator brochures, and clinical study reports.

3. Address medical inquiries from study sites, ensuring that research complies with scientific and ethical standards.

4. Establish and maintain academic relationships with key opinion leaders (KOLs) in the field; organize advisory boards and academic roundtable discussions.

5. Track, collect, and analyze domestic and international clinical research developments and data relevant to the company’s products.

Qualifications:

1. Master’s degree or above in Clinical Medicine, Life Sciences, or related fields; Ph.D. preferred.

2. 3–5 years of experience in medical affairs, clinical research, or related fields.

3. Familiarity with clinical research content and processes; good knowledge of GCP.

4. Strong English skills preferred.

Responsibilities:

1. Design and conduct preclinical pharmacokinetic (PK) study protocols and experiments.

2. Perform in vivo studies on drug absorption, metabolism, distribution, and excretion across different animal species.

3. Carry out in vitro PK studies, including plasma stability, plasma protein binding, liver microsomal metabolic stability, MDR1-MDCK permeability assays, etc.

4. Analyze experimental results and prepare study reports; strong English skills required.

Qualifications:

1. Bachelor’s degree or above in Pharmacokinetics, Pharmacology, Physiology, or related fields; at least 1 year of relevant work experience, with CRO experience preferred.

2. Strong execution, communication, and problem-solving skills.

3. Honest, proactive, with strong teamwork spirit, high sense of responsibility, and professional dedication.

Responsibilities:

1. Conduct monitoring visits at assigned clinical trial sites in accordance with GCP and the company’s SOPs, ensuring that trial data are authentic, accurate, complete, and compliant with regulatory requirements.

2. Assist with trial site initiation, execution, and close-out, including investigator selection, site initiation meetings, and trial progress monitoring.

3. Perform regular on-site and remote monitoring to ensure trials proceed as planned, promptly identifying and resolving issues.

4. Prepare and submit monitoring reports, document findings, and follow up on corrective actions.

5. Maintain strong relationships with trial sites, supporting investigators and site teams to achieve study objectives.

6. Ensure patient rights and safety are protected during trials, in line with ethical principles.

7. Support communication with ethics committees, including document submission and follow-up.

8. Collaborate with the quality management team during inspections and audits to ensure project compliance.

Requirements:

1. Bachelor’s degree or above in medicine, pharmacy, life sciences, or related fields.

2. At least 1 year of monitoring experience; prior Phase III trial or oncology experience preferred.

3. Familiar with regulations and guidelines for drug clinical trials, with solid knowledge of ICH-GCP.

4. Excellent communication, coordination, and teamwork skills; able to handle multiple tasks efficiently.

5. Strong learning ability, sense of responsibility, and resilience under pressure.

6. Willingness to travel as required.

Responsibilities:

1. Review documents, records, and reports, conduct deviation investigations and handle follow-up.

2. Perform routine on-site inspections and record checks.

3. Collect and organize regulatory requirements.

4. Participate in and assist with laboratory experiments.

Qualifications:

1. Proficient in the use of major analytical instruments such as HPLC, GC, atomic absorption spectrometer, particle size analyzer, with knowledge of operating precautions; capable of compiling and analyzing data and identifying abnormal results.

2. Familiar with routine analytical instruments such as UV spectrophotometer, polarimeter, melting point apparatus, IR spectrometer, TLC, and dissolution apparatus, with understanding of operational details.

3. Experience in method validation, cleaning method development and validation, drafting/reviewing quality documents, and reviewing test records/reports, with strong document review skills.

4. Strong ability to analyze and address laboratory deviations, OOS (Out of Specification), and AD (Analytical Data) issues.

5. Solid knowledge of pharmacopeia, GMP guidelines and principles, and regulations related to quality testing.

6. Bachelor’s degree or above in Pharmaceutical Engineering, Pharmaceutics, Pharmacy, or related disciplines.

7. At least 3 years of experience in compound characterizations, able to independently test APIs, excipients, and finished products; candidates with experience in drafting/reviewing documents and method validation are preferred.

Responsibilities:

1. Responsible for drafting production documents for Solid Dosage Workshop 1, including but not limited to process procedures, batch records, and cleaning evaluation reports.

2. Responsible for reviewing batch records for the position, and for drafting and reviewing GMP-related documents for the workshop.

3. Responsible for on-site workshop management.

Qualifications:

1. At least 2 years of experience as a process technician or administrator in a GMP workshop.

2. Familiar with all operational procedures of solid dosage workshops.

3. Proactive work attitude with the ability to coordinate collaboration across different positions.

Responsibilities:

1. Perform duties in the solid dosage workshop, including tableting, granulation, capsule filling, coating, packaging, line cleaning, basic equipment maintenance, and batch record preparation.

2. Follow supervisors’ instructions, follow GMP standards carefully, and carry out production in compliance with SOPs and position requirements.

Qualifications:

1. Associate degree or above.

2. Familiarity with company and department documents, as well as GMP regulatory requirements.

3. Proficient in production processes and equipment operation for this position.

Responsibilities:

1. Review batch records for commercial production release.

2. Supervise production at contract manufacturing organizations (CMOs).

3. Conduct on-site audits of suppliers.

4. Review and manage qualification documents and files of purchasing units.

5. Assist project QA with daily records and logbook issuance.

Requirements:

1. College degree or above in pharmacy or related fields.

2. At least 1 year of QA or workshop experience in a pharmaceutical company; experience with oral solid or liquid non-sterile dosage forms preferred.

Responsibilities:

1. Maintain and develop distribution agents in sales channels (e.g., pharmacy chains, private clinics, independent pharmacies, etc.).

2. Report market trends to supervisors and provide constructive recommendations.

3. Build strong client relationships and maintain the company’s positive image.

4. Achieve sales targets and complete other tasks assigned by management.

Qualifications:

1. Associate degree or above in Pharmacy, Marketing & Sales, Retail Management, or related fields.

2. Experience in pharmaceutical retail or channel management; candidates with established channel resources are preferred. Must be willing to travel; base location can be in North China or Southwest China.

3. Proficient in Microsoft Office and other office software.

4. Strong communication and coordination skills, with a good team spirit.

Responsibilities:

1. Responsible for the daily operation, maintenance, repair, and technical upgrades of utility equipment;

2. Operate HVAC systems, chilled water systems, air compressors, vacuum pumps, purified water, clean steam, steam generators, and other equipment to ensure compliance with GMP requirements, prevent violations, and guarantee safe production;

3. Participate in energy consumption management.

Requirements:

1. Secondary technical school diploma or above in chemical machinery, HVAC, electromechanical engineering, or related mechatronics disciplines;

2. At least 2 years of relevant experience in utility equipment management or maintenance within a pharmaceutical manufacturing enterprise.