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. **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. **Locations** Tianjin, China **Worker Type** Employee **Worker Sub-Type** Regular **Time Type** Full time