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CMC pharmaceutical CMC Regulatory Affairs

塩野義製薬株式会社

  • pharmaceutical regulations
  • CMC Regulatory Affairs
  • CMC pharmaceutical
  • Sumitomo Dainippon Pharma
  • low-molecular-weight pharmaceutical
  • global CMC pharmaceutical development
  • Work Location Osaka
  • Company employee count 1,001 to 10,000

Company Info

Sumitomo Pharmaceuticals aims to create a new platform in 2030 to create the future of health care. As a data engineer, you will collect and manage internal and external data, establish a data management system at the company-wide level, and develop plans and strategies related to data utilization in the healthcare domain, including business plans and expansion strategies.

Job Summary

In the position of CMC Regulatory Affairs for CMC pharmaceuticals, we are responsible for the development, approval, and management of CMC pharmaceuticals, as well as the overall management of low-molecular-weight pharmaceuticals. We provide support for the latest product quality in global product development, understand the regulations for pharmaceutical development in global markets, and provide skills to support global CMC pharmaceutical development.

Duties

Responsible for the development, approval, and management of CMC pharmaceuticals, as well as the overall management of low-molecular-weight pharmaceuticals. Specifically, understanding the regulations for pharmaceutical development in global markets, and providing skills to support global CMC pharmaceutical development.

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CMC pharmaceutical CMC Regulatory Affairs

塩野義製薬株式会社

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