Pharmaceutical Regulatory Affairs Expert
中外製薬株式会社
- GMP
- Manufacturing
- Product quality management
- Pharmaceutical products
- regenerative medicine
- QMS
- pharmaceutical regulations
- Medical Devices
- pharmaceutical and medical device development
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Tokyo
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1,001 to 10,000
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Company Homepage
Company Info
Job Summary
In the position to be recruited, it is possible to contribute to the development of pharmaceutical products and medical devices, and to conduct related surveys related to the development and marketing of pharmaceutical products, and to manage documents related to domestic and foreign regulatory authorities, and to contribute to a wide range of pharmaceutical business.Duties
As a pharmaceutical regulatory affairs expert, conduct surveys related to the development of pharmaceutical products, medical devices, and regenerative medicine, and manage internal coordination, and manage documents related to domestic and foreign regulatory authorities, and conduct GMP/QMS/GCTP compatibility surveys, and conduct surveys related to manufacturing and sales of pharmaceutical products in foreign countries, and conduct various business such as product development and project management.Login to see all information about offers.
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