You will have a direct impact on patient safety, product quality, and regulatory compliance, delivering meaningful work that is highly visible across the organization
Job Summary
You will have a direct impact on patient safety, product quality, and regulatory compliance, delivering meaningful work that is highly visible across the organization.
This role offers you broad cross-functional exposure, ownership of complex investigations, and the opportunity to act as a subject matter expert while driving continuous improvement.
Takeda is focused on creating better health for people and a brighter future for the world.
Matching Summary
You will have a direct impact on patient safety, product quality, and regulatory compliance, delivering meaningful work that is highly visible across the organization.
Skills & Requirements
Must-have
Manage product quality complaints end-to-end
Ensure complaint handling compliance
Assess complaints for patient safety
Coordinate cross-functional investigations
Act as quality SME
Drive continuous improvement of processes
Nice-to-have
Patient-oriented, innovation-driven company
Meaningful work with high visibility
Broad cross-functional exposure
Flexible working arrangements
Development opportunities
Key Requirements
Bachelor's degree and 5–9 years of experience
Strong knowledge of cGMP and regulatory requirements
Understanding of EU and FDA requirements
Relevant experience in complaint handling and quality investigations
Good understanding of combination product manufacturing