By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
OBJECTIVE:
The responsibility of this role is to maintain continuous improvement of quality as a foundation of Takeda’s Corporate Vision, Mission and Values and ensure all of the local GxP activities are in compliance with Health Authority requirements, Takeda requirements and standards.
ACCOUNTABILITIES:
1. Maintain a comprehensive Quality Management System (QMS) to achieve Takeda’s quality objectives. These include but not limited to:
2. Manage product disposition and prepare Product Quality Review
3. Support cross function activities / projects when required ensuring quality regulations and requirements are followed.
4. Support in driving Quality Culture and implementing quality risk management.
5. Communication with the health authorities in timely and effective manner ensuring smooth release of products and efficient resolution of critical quality issues requiring health authorities’ approval.
QUALIFICATIONS:
TRAVEL REQUIREMENTS: upon requirement
About Takeda Pharmaceuticals
Takeda is a global, research and development-driven pharmaceutical company committed to bringing better health and a brighter future to patients by translating science into life-changing medicines.
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