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Operation QA Technician [Quality Department]
Negotiable
Education：
本科
|
Work experience：
1-3年
|
Number of recruits：
1
Job description
1. Supervise the implementation of on-site processes in the workshop and the implementation of GMP.
2. Responsible for the related work of listed products. Such as quality files, return surveys, product quality analysis, etc.
3. Responsible for the development of CAPA related work of deviation change, as well as the summary of various data, and analyze related trends.
4. Responsible for reviewing batch production records, batch inspection records and supervising the disposal of substandard products, and responsible for the release of raw liquid products.
5. Responsible for the review of relevant documents, and participate in various quality audit self-inspection and improvement activities.
6. Track the construction progress of new engineering projects. Complete the work assigned by the superior leadership on time, quality and quantity.
Education background: Biochemistry, bioengineering, pharmacy and other related majors, bachelor degree or above.
Work experience: at least 1 year of work experience in QA of pharmaceutical production quality control
Skills: Have a strong sense of responsibility and good coordination and communication skills, be familiar with domestic and foreign industry regulations and guidelines, have the ability to identify and solve risk problems, have good organizational coordination and statistical analysis skills, and be able to work efficiently and improve the team Build capacity.
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Maybe you want to know more:
Jilin Province GenPEG Pharmaceutical Co.,Ltd.
Service Hotline：400-8200469
Company email：jinpg@genscigroup.com
PEG Sales Dedicated Email：salespeg@genscigroup.com
Company address: Xiashi Economic and Technological Development Zone, Dunhua City, Yanbian Prefecture, Jilin Province
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