Independently carries out activities to ensure that non-clinical Research study activities are in compliance with applicable regulations and Takeda requirements
Job Summary
Independently carries out activities to ensure that non-clinical Research study activities are in compliance with applicable regulations and Takeda requirements.
Leads supplier quality oversight/qualification activities for externalized non-clinical studies and partners with stakeholders to advance quality, compliance, and data integrity principles.
Offers a comprehensive benefits package including allowances, annual salary increases, bonuses, and various paid leaves.
Matching Summary
Independently carries out activities to ensure that non-clinical Research study activities are in compliance with applicable regulations and Takeda requirements.
Skills & Requirements
Must-have
GLP compliance
non-clinical study oversight
supplier quality management
data integrity assurance
regulatory submission support
Nice-to-have
collaboration and relationship building
proactive problem identification
subject matter expertise
diverse and inclusive organization
Key Requirements
Bachelor's degree in Chemistry, Biology, Engineering or related field
Minimum 5 years pharmaceutical industry experience
GLP personnel QA experience
Experience in regulatory submission relevant studies
Business level Japanese speaking, writing, and reading