Site QA
4500-6000
Responsibilities:
1. Be responsible for the quality control of the whole production process in the area under its jurisdiction (monitoring of each key quality control point, confirmation of production environment, specification of production personnel, sampling and inspection, etc.), ensure that all key points in the whole production process are controllable, and make quality supervision records;
2. Responsible for production order review, material review and site clearance inspection after production;
3. Responsible for checking the filling of batch production records and other relevant records, and organizing the revision and collection;
4. Collect and sort out the defects found in the monitoring process and the quality information in the production process;
5. Participate in the deviation handling of the production process, investigate the cause of the complaint, control the change risk, and follow up the implementation of corrective and preventive measures;
6. Daily monitoring of environment, water system and surface microorganism in production clean area;
7. Assist QA director to do other work arrangements of the department.
Requirements:
1. College degree or above, major in pharmacy, biology, pharmaceutical engineering, etc;
2. At least 1 year QA experience in pharmaceutical production;
3. Proficient in office software;
4. Experience in pharmaceutical production and quality management is preferred.
Company address: Floor 4 and Floor 5 (1) of Building 3, Phase 3.1, Wuhan Optics Valley International Biomedical Enterprise Accelerator, 388 Gaoxin 2nd Road, Donghu New Technology Development Zone, Wuhan City
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