Quality management (raw material) duties
協和キリン株式会社
- GMP
- Quality management
- cGMP
- PIC/S
- Bio-technology
- Pharmaceuticals
- analytical chemistry
-
Gunma
-
1,001 to 10,000
Company Info
The collaborative Kirin Group is engaged in the development of pharmaceutical products, and is committed to promoting health. We aim to realize a prosperous life, and seek non-smokers.Job Summary
As a responsible person for the quality management of pharmaceutical raw materials, you will be responsible for the quality management operations at the GMP management test room, as well as the introduction of business improvement and new analytical technologies, and compliance with the latest regulations. We seek individuals with a wide range of interests in medicine and pharmaceuticals, a rich imagination, and a spirit of exploration, as well as a willingness to seek knowledge and problem-solving abilities.Duties
In the quality management (raw material) department of pharmaceuticals, you will be responsible for the following tasks. As a person responsible for the quality management of pharmaceutical raw materials, you will be responsible for the quality management operations at the GMP management test room. Specifically, you will be involved in the overall management of raw material quality control, business improvement, inspection/audit, application for certification documents, new registration and changes, introduction of new analytical technologies, and compliance with pharmaceutical regulations. It is also possible to refer to overseas pharmaceuticals and conduct the latest PIC/S GMP and cGMP compliance, and to conduct inspections and audits including overseas organizations, and to contribute to the provision of high-quality pharmaceutical products to people around the world.Login to see all information about offers.
By registering with LabBase Plus you...
- can view all offer information,
- receive notifications of new offers,
- possibly be scouted by corporations
Registration takes roughly 2 minutes