bd半岛体育·(中国)官方网站

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.

1.Experimental reagents and consumables purchase application, receiving, storage, issuance, inventory and other inventory management.

2. Receive and manage the finished products produced by the clinical trial production department

3. Receiving, storage, distribution and inventory management of plasmids and strains

4.Responsible for the management of the whole life cycle of the company's laboratory equipment, instrument and equipment measurement, calibration, repair, utilization statistics; logo management; responsible for the validation and revalidation of equipment according to GMP requirements, routine maintenance, inspection and repair of equipment

5. Collect, establish and maintain equipment maintenance contact files, inspection files, contracts, laboratory records, etc..

6. Laboratory safety officer related work.

7.Ability to work closely with all groups in the lab and be able to solve problems in a timely and effective manner during the process

8.Timely completion of rectification according to internal/external audit requirements

9. Emergency handling of emergencies, clear logic, able to deal with complicated matters

10. Other work arranged by superiors

1.With college degree or above in biology, medicine, chemistry or other related majors; more than 1 year in laboratory operation or management related work, with work experience in pharmaceutical and CRO companies, and participation in GMP validation work is preferred.

2. have laboratory equipment management and maintenance related work experience; familiar with the basic operation process of biochemical laboratory is preferred.

3. Proficiency in using daily office software (word, excel, PPT).

4. Conscientious, careful, responsible and patient in daily work, with a strong sense of responsibility and team spirit.

5. Have some SOP writing ability and good coordination and communication skills.