Responsibility

1、Familiar with GMP and pharmaceutical regulations, confirm the GMP implementation status of each department;

2、Supervise the accuracy and timeliness of filling in on-site production and inspection records;

3、Participate in the revision/review of product process specifications, production records, and various operating procedures;

4、Other tasks: Responsible for other daily work of the quality department;

5、Other work tasks assigned by superiors.

Requirement

1、Bachelor's degree or above, majoring in chemical or pharmaceutical related fields;

2、Familiar with ICHQ7 and GMP quality management systems, proficient in drug quality management knowledge;

3、Strong analytical and judgment skills, logical thinking ability, execution ability, understanding and feedback ability;

Responsibility

1、Responsible for company product registration related business;

2、Registration application and progress tracking of drugs;

3、Pay attention to the latest drug registration policies and prepare registration application documents according to the new policy adjustments;

4、Participate in and cooperate with the Quality Department to complete official and customer written and on-site audits;

5、Responsible for other daily work of the registration department and other tasks assigned by superiors.

Requirement

1、Bachelor's degree or above, major in chemical or pharmaceutical related fields, College English Test Band 4 or above;

2、Familiar with various national laws, regulations, and national and industry standards related to pharmaceutical companies;

3、Work meticulously, rigorously, proactively, with strong organization, good sense of responsibility and teamwork spirit.

Responsibility

1、Strictly follow relevant standards and inspection procedures for sampling, testing, and retention, and accurately, clearly, and timely keep relevant records and issue inspection reports;

2、Participate in the development, transfer, validation, and confirmation of analytical methods;

3、Participate in the investigation of deviations, inspection deviations, and OOS that occur during the testing process, participate in the investigation of product quality returns, complaints, and the implementation of changes;

4、Responsible for other daily work of the quality inspection center and other tasks assigned by superiors.

Requirement

1、College degree or above, majoring in chemical or pharmaceutical related fields;

2、Proficient in operating physical, chemical, gas, and liquid detection instruments, familiar with GMP and pharmaceutical regulations;

3、Good sense of responsibility and teamwork spirit.

Responsibility

1、Participate in the research and development of new products, conduct pilot production and trial production of new products and technologies;

2、Improve the process of old products, including small-scale research and development and trial production;

3、Complete experimental records, experimental reports, etc., and cooperate in writing relevant application materials and records;

4、Responsible for other daily work of the R&D center and other tasks assigned by superiors.

Requirement

1、Bachelor's degree or above, majoring in chemical or pharmaceutical related fields, with a solid foundation in organic synthesis;

2、Strong analytical and problem-solving skills, with good professional English translation skills preferred;

3、Passionate about laboratory work, with a strong sense of responsibility and teamwork spirit