The department is responsible for quality assurance in the development of investigational medicinal products, covering various modalities such as small molecules, peptides, antibodies, and oligonucleotides
Job Summary
The department is responsible for quality assurance in the development of investigational medicinal products, covering various modalities such as small molecules, peptides, antibodies, and oligonucleotides.
Key responsibilities include monitoring GMP compliance, providing QA perspectives on development strategies, approving manufacturing and testing methods, and managing changes and deviations.
Takeda is a global values-based, R&D-driven biopharmaceutical leader committed to creating a diverse and inclusive organization.
Matching Summary
The department is responsible for quality assurance in the development of investigational medicinal products, covering various modalities such as small molecules, peptides, antibodies, and oligonucleotides.
Skills & Requirements
Must-have
GMP compliance monitoring
Investigational medicinal product development
Business level Japanese
Supplier GMP audits
Nice-to-have
Global development program experience
Proactive problem-solving
Negotiating mutually beneficial solutions
Key Requirements
8+ years of QA experience in investigational drug development/manufacturing
Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or related science