Pharmaceutical product analysis and management
沢井製薬株式会社
- GC
- HPLC
- pharmaceutical raw materials
- ICH
- standards
- pharmaceutical formulations
- quality evaluation
- test methods
- biological equivalence tests
- dissolution tests
- development of evaluation methods related to pharmaceutical product quality
- application for pharmaceutical product recognition
- ¥4,500,000 - 7,000,000
- Osaka
- 1,001 to 10,000
- Company Homepage
Company Info
Conducting research and development of pharmaceutical products, promoting the improvement of new evaluation methods and stable supply, and promoting the improvement of pharmaceutical product development and business improvement as a responsible person for pharmaceutical product analysis.Job Summary
As a responsible person for pharmaceutical product analysis, conduct research and development of generic drugs and formulations, creation of quality and efficacy evaluations, biological equivalence tests and dissolution tests, and handling of application data creation and regulatory affairs, and promote the development of new evaluation methods and business improvement for pharmaceutical product development, and promote the progress of quality assurance, compliance, and team management.Duties
As a responsible person for pharmaceutical product analysis, conduct research and development of pharmaceutical products, and handle a wide range of tasks such as creation of quality and efficacy evaluations, biological equivalence tests, dissolution tests, and application data creation and regulatory affairs. In addition, in the short term, handle specific tasks related to generic drugs and formulations, expand the scope of work, achieve the development of new evaluation methods for pharmaceutical product development, and promote the progress of quality assurance, compliance, and team management. In addition, inquiries will be made about pharmaceutical affairs and product quality assurance within the company.Login to see all information about offers.
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