■ Responsible for quality assurance operations in the pharmaceutical manufacturing and sales industry. 【Details】Creation and maintenance of quality standard documents such as GQP documentation / Management of shipment to the market / Response to quality information from the market / Collaborative work with the research and development center (regulatory responses / DI responses / information on packaging materials, etc.) / Management and supervision of manufacturers (contract conclusion / confirmation of GMP operational status / change management / deviation management, etc.)【Attraction of the job】The company was the first in Japan to launch 'artificial kidney perfusion raw liquid.' It is possible to work with a sense of fulfillment as you engage in quality assurance for products that support many patients' lives. As a listed company on the prime market, we deliver safety and security to the market. ※ The company culture values each employee. ※ There has been no restructuring in the past. You can work with peace of mind in the long term.
The above information is a public job ad. This job ad is neither an offer nor a contract.
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