Laboratory technician
Release Date:
2020-04-22
Job Requirements: 1. Bachelor’s degree or above in Pharmacy, Chemistry, or a related field; 2. At least 3 years of work experience in the quality department of a pharmaceutical company; 3. Detail-oriented, meticulous, and highly responsible.
Job Responsibilities:
1. Raw Material Sampling:
Upon receipt of the incoming goods inspection request form, the laboratory technician shall proceed to the designated sampling location to collect samples of the incoming raw materials. Sampling shall be conducted in accordance with the respective material-specific sampling procedures to ensure that the collected samples are representative. Following completion of sampling, the sample collection record shall be completed based on the actual sampling results.
2. Sample Registration
Laboratory analysts shall promptly record samples in the Sample Collection Registration Form. Raw materials must be retained as samples until the completion of production. Sample retention shall be carried out in accordance with the Sample Retention Management System. Retained samples must be registered in a timely manner, with strict verification that the physical samples match the corresponding records, and their integrity must be maintained throughout the retention period. No samples may be loaned out or exchanged without prior approval.
3. Sample Inspection
Finished-product inspection shall be conducted batch by batch in accordance with the specified requirements, and the inspected samples shall be sealed and stored after completion of the inspection.
4. Fill in the record
During the inspection process, laboratory technicians shall complete the inspection records at all times. The inspection records must be filled out accurately and in accordance with the specific procedures, with clear and neat handwriting on each page, and no unauthorized alterations are permitted.
5. Issuance of the Inspection Report
The issuance of inspection reports shall be strictly based on the data recorded in the inspection records. No arbitrary alterations are permitted, and inspectors shall verify the inspection data to ensure its accuracy and authenticity.
6. Submission of Inspection Report
Submit the completed inspection report to the head of the relevant department.
Job Requirements:
1. Bachelor’s degree or higher in pharmacy, chemistry, or a related field;
2. At least 3 years of work experience in the quality department of a pharmaceutical company;
3. Meticulous and conscientious in work, with a strong sense of responsibility.
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