Quality Assurance

■ 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.


SalaryJPY 4500K - JPY 7000K
Working Hours08:00 to 17:00
Work TypeFULL_TIME
Applicant needs to be in Japan
Applicant needs to speak Japanese
Is accommodation included?
Is food included?
Visa RequirementsNot specified
Minimum Commitment

Language Requirements

Business Conversation Level (TOEIC 735-860) English
Fluent (JLPT Level 1 or N1) Japanese

Qualifications

Best to have experience related to GQP, but knowledge can be acquired through work

Requirements

Experience in quality assurance or quality control of pharmaceuticals or pharmaceutical raw materials
Knowledge of GMP
Knowledge of regulations such as Pharmaceutical and Medical Device Act / GQP / GMP
Ability to translate English reports

The above information is a public job ad. This job ad is neither an offer nor a contract.

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