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This is a wonderful opportunity to join the Manufacturing Investigation Team where you will be exposed to a multifaceted environment within manufacturing across; Purification, Filling, Packaging, Engineering, and Environmental Monitoring. As the Deviation Associate Specialist you will lead investigations related to a variety of risks. Responsible for investigating and detailing the root causes of an event, writing investigation reports, and coordinating the development and implementation of action plans necessary to avoid reoccurrence. Handle deviations promptly and establish effective communication with vital team members across the departments.
On a personal level, you are open-minded, proactive, and eager to learn. An individual who shows curiosity and enjoys solving problems with a creative approach. More importantly, possesses excellent organizational skills, attention to detail, and the ability to collaborate effectively with a phenomenal interpersonal skills to communicate internally.
We will make sure you get all the training and development opportunities you need to become the best in your field.
At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
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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