Manufacuturing science Engineer
応募 後で応募 求人ID R0159437 掲載日 07/30/2025 Location:Tianjin, ChinaBy 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’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Job Title: Manufacturing Science Engineer
Location: Tianjin, China
About the Role:
Ensure the smooth execution of the “China for China” new product introduction and transfer project at Takeda’s Tianjin plant.
How You Will Contribute:
Technology Transfer: Participate in new product technology transfers, including process research, evaluation, and implementation; draft related technical documents. Process Optimization and Improvement: Analyze production processes, propose technical improvement plans, and optimize processes to enhance production efficiency and product quality. Problem Analysis and Resolution: Troubleshoot issues in production, provide technical support, and quickly resolve technical problems related to processes and equipment. Document Preparation: Write and review relevant technical documents, such as validation protocols, SOPs, deviation reports, ensuring compliance with GMP and regulatory requirements. Validation Support: Support process and cleaning validation efforts, ensuring compliance in process and product validations. Cross-Department Coordination: Collaborate with R&D, quality, production, and other departments to ensure smooth technical communication and support. Regulatory Compliance: Ensure technical solutions and operations align with pharmaceutical regulatory requirements and internal company standards. Audit Support: Assist with the completion of internal and external audits and address corrective and preventive actions in a timely manner.
What You Bring to Takeda:
Education: Bachelor’s degree or above, with a background in pharmacy or chemistry. Work Experience: At least 3 years of experience in process technology or technology transfer in pharmaceutical companies, particularly in packaging technology transfer; familiar with validation and technical transfer documentation. Professional Knowledge: Strong GMP foundation; familiar with pharmaceutical production and technology transfer processes with deep knowledge of regulations to ensure compliance in technical transfers. Skills: Strong analytical and problem-solving skills, excellent organizational and team collaboration abilities. English Proficiency: Proficient in English (listening, speaking, reading, writing) with the ability to communicate independently and smoothly with international collaborators.