Principal Manager, R&D GMP Pharmaceutical Sciences Quality EU - Lexington

Only for registered members Lexington, United States

3 days ago

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Job summary

The Principal Manager
R&D GMP Pharmaceutical Sciences Quality EU & US
provides Quality oversight across Takeda's investigational medicinal product development lifecycle,
from early clinical development through commercialization.

Responsibilities

  • Oversee final release and disposition of Clinical Trial Material across multiple modalities and complex development programs.
  • Review and approve batch documentation...

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