Description
This job requires native level Japanese proficiency in writing, reading and speaking.
Takeda is always centered on the patient, promoting innovation to enrich their lives. We strive to provide each employee with growth opportunities tailored to their abilities and passion. Will you join us in contributing to people's lives around the world and striving for further growth and success?
Takeda is a global company with approximately 60,000 employees working in over 54 countries and regions. We share a belief that all employees want to make the world a better place, and embody Takeda-ism (Sincerity: Integrity, Honesty and Perseverance) in our daily work. As a 238-year-old research-driven pharmaceutical company, we unite under our traditional values and contribute to the health and medical future of people through the creation of outstanding medicines.
Department Introduction
The Hikari Plant is Takeda's main production plant located in Hikari City, Yamaguchi Prefecture, and plays an important role as a core plant in our global supply network, shipping products not only domestically but also globally.
The Sterile Manufacturing Department has functions for manufacturing injectable products and process support, producing high-quality products (vial products, dual-chamber syringe), and conducting continuous process improvement and establishing new manufacturing lines.
Job Responsibilities
You will be responsible for the following tasks related to the manufacture of injectable products:
- Injection product manufacturing operations
- Continued engineering improvement
- Establishing and educating appropriate SOPs
- Validation/Qualification of manufacturing processes and equipment
- Response to inspections by regulatory authorities
- New equipment and process design and establishment
- Promoting the advancement of digital technology and other new technologies for process optimization
Application Requirements
We are looking for candidates with the following qualifications and experience:
- High school graduate or higher with relevant work experience
- Candidates with the following work experience or equivalent experience:
- Manufacturing of pharmaceutical products (regardless of product type)
- GMP-related knowledge
Desirable Qualifications
We welcome candidates with the following qualifications:
- University graduates (pharmaceutical, engineering, science, agriculture, chemistry, or mechanical engineering)
- Candidates with the following experience:
- New equipment and process design and establishment
- Response to inspections by regulatory authorities
Working Hours
Your assigned shift will be either two-shift or three-shift work.
- Microcapsule G: 7:00 AM - 9:00 PM
- Syringe product G: 6:00 AM - 12:00 AM
- Vial product G: 8:00 AM - 4:45 PM
Please note that your schedule may change every month.
Employment Status
Regular Employee
Work Location
Hikari Plant
Takeda Compensation and Benefits Summary:
Important Notice concerning working conditions:
- It is possible the job scope may change at the company's discretion.
- It is possible the department and workplace may change at the company's discretion.
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