Job Requirements:

1, Biomedical or related major, doctor or above;

2. Rich working experience;

Job Responsibilities:

1. System document management: document formulation, issuance, cancellation and preservation;

2. Supervise relevant departments and personnel to implement regulations, rules and norms of medical devices to ensure quality

3. Assisted the quality manager to carry out quality management training;

4. Completed product acceptance and process inspection;

5. Participate in the implementation of verification and validation;

6. Other quality-related matters.

Job Requirements:

1. Bachelor degree or above in life science;

More than 1 year quality work experience;

3. Familiar with the production and sales process of medical devices and relevant rules of ISO13485;

4. Good team spirit and rigorous working attitude, able to work under pressure.

Job Responsibilities:

Responsible for drug analysis products, including residual DNA quantification, mycoplasma detection, microbial identification, virus detection, protein residue quantification and automated sample preparation, antibiotic detection, IPTG detection, organic solvent detection, peptide spectrum analysis, terminal amino acid analysis, etc

Job Requirements:

1. Bachelor degree or above in biomedical or related field.

Job Responsibilities:

1. Responsible for the research and development of bio-engineering products, and responsible for the quality, schedule and cost.

Job Requirements:

1. Bachelor degree or above in biomedical or related field.

Job Responsibilities:

1. Isolation and purification of protein drugs (vaccines) and development of purification process in small scale;

2. Pilot production of protein drugs (vaccines);

Job Requirements:

1. Bachelor degree or above in biomedical or related field.

Job Responsibilities:

1. Coordinate the construction of software system for GMP certification of existing workshops and new pharmaceutical factories in the future, organize the preparation of software system data for GMP certification, and standardize the operation and management of the company according to GMP certification standards;

2. Responsible for the company's implementation and enforcement of drug production laws and regulations, responsible for the establishment of quality assurance management system and the organization of implementation;

3. Establish deviation treatment management system and review deviation treatment records. Responsible for organizing quality system evaluation of major material suppliers. Responsible for supervising the stability inspection of materials, products and intermediate products;

4. Responsible for implementing supervision and urging the completion of product quality review analysis report, and rectification of defects suggested by product quality review summary;

5. Responsible for personnel and organization training, personnel health management, plant and facilities, equipment, materials, public systems, production workshop, warehouse, quality control and other management.

Job Requirements:

1, Pharmacy or related major, bachelor degree or above;

2. Rich experience.

Job Responsibilities:

1. Familiar with the application of cell biology and molecular biology;

2. Responsible for the research and development of cell biology and molecular biology products;

3. Participated in the research of cell biology and molecular biology products and assisted in the preparation of research reports and other relevant technical documents.

Job Requirements:

1, Biomedical or related major, master degree or above;

2. Rich experience.

Job Responsibilities:

1. System document management: document formulation, issuance, cancellation and preservation;

2. Supervise relevant departments and personnel to implement regulations, rules and norms of medical devices to ensure quality

3. Assisted the quality manager to carry out quality management training;

4. Completed product acceptance and process inspection;

5. Participate in the implementation of verification and validation;

6. Other quality-related matters.

Job Requirements:

1. Bachelor degree or above in life science;

No experience is required.

3. Familiar with the production and sales process of medical devices and relevant rules of ISO13485;

4. Good team spirit and rigorous working attitude, able to work under pressure.

Job Responsibilities:

1. System document management: document formulation, issuance, cancellation and preservation;

2. Supervise relevant departments and personnel to implement regulations, rules and norms of medical devices to ensure quality

3. Assisted the quality manager to carry out quality management training;

4. Completed product acceptance and process inspection;

5. Participate in the implementation of verification and validation;

6. Other quality-related matters.

Job Requirements:

1. Bachelor degree or above in life science;

No experience is required.

3. Familiar with the production and sales process of medical devices and relevant rules of ISO13485;

4. Good team spirit and rigorous working attitude, able to work under pressure.