[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Takeda Pharmaceutical jobs](https://jobs.opennash.com/companies/takeda-pharmaceutical/) · [Search jobs](/search/) Takeda Pharmaceutical # Senior Manager, Regulatory Affairs, Onco Manager or lead Legal & Compliance Listed on Takeda Pharmaceutical’s official careers site. Listed as of October 18, 2026. Check that it is still open and apply there. [Apply on Takeda Pharmaceutical’s careers site →](https://jobs.takeda.com/job/beijing/senior-manager-regulatory-affairs-onco/1113/96837731312) [OpenNash Jobs](https://jobs.opennash.com/) / [Takeda Pharmaceutical](https://jobs.opennash.com/companies/takeda-pharmaceutical/) / Senior Manager, Regulatory Affairs, Onco ## Job description 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 Accountabilities: In accordance with the company’s product launch strategy and department’s work plan, take full responsibility of the product registration and application for approval and develop the plan by stage. Contribute to decision making on drug registration leading to minimal registration timeline. May lead a project team or initiative within department or cross-functions/divisions. Provides technical leadership to business. Summarize product registration related materials with coordination among head office, factory, Sales & Marketing. Provide corresponding support for the sales in China market. In accordance with the plan of product registration and application for approval, manage the necessary materials and information during the process and track and summarize the progress. Be responsible for submission of complete and qualified product application data to drug regulatory authorities, coordination of raw data review and on-site assessment. Manage and archive examination and registration materials and other relevant documents. Provide necessary support to the preparation and implementation of clinical trial. Establish influential relationships with key regulatory authority individuals and KOLs in relevant fields, such as SFDA, CDE, NIFDC, PIDC etc. Monitor regulatory environment and collect important information such as regulations, guidelines, competitive products etc. Establish and maintain internal/external channels of communication. Ensure regulatory activity is in compliance with authority and Takeda policy. Coordinate with the establishment of internal SOP and system. Others assigned by line manager. ### Education & Competencies (Technical and Behavioral) Level of Education: Bachelor’s degree or above majored in medicine or pharmacy. ### Working Experience in Relevant Field >7 years related work experience Professional Knowledge and Skills: Skilled in using computer office software. Good English or Japanese in listening, speaking, reading and writing. Be familiar with the laws and regulations of drug administration and registration management, stronger professional competency, excellent communication skill and leadership. Teamwork and collaboration. Locations Beijing, China Worker Type Employee Worker Sub-Type Regular Time Type Full time ## At a glance - Posted by the employer: Not stated - First seen by OpenNash: Jul 16, 2026 - Last checked: Oct 18, 2026 - Listed for: 94 days[Apply on Takeda Pharmaceutical’s careers site →](https://jobs.takeda.com/job/beijing/senior-manager-regulatory-affairs-onco/1113/96837731312) ## More jobs at Takeda Pharmaceutical ### [Associate Director, EU Regulatory Lead Neuroscience](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/54a54507042b317ee129/) ### [Associate Director, Global Regulatory Affairs CMC](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/33c7199c34eef68b732e/) ### [Associate Director, Global Regulatory Affairs, Precision Medicine & Digital Health](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/bef1b6fbdbb89bd9db19/) ### [Associate Director, Global Regulatory Labeling Strategy](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/649d7e273229bbf157a9/) ### [Associate Director, Global Regulatory Lead, Oncology](https://jobs.opennash.com/companies/takeda-pharmaceutical/jobs/f838cb9b48419bf9c503/) ## Similar jobs at other companies ### [Utility Regulatory Affairs Senior Advisor](https://jobs.opennash.com/companies/edison-international/jobs/e65e0246ae95ee67c55a/) Edison International ### [Senior Manager, Global Regulatory Affairs](https://jobs.opennash.com/companies/otsuka-holding/jobs/20170b14c753a6dc315f/) Otsuka Holding ### [Regulatory Affairs Portfolio Manager](https://jobs.opennash.com/companies/novartis/jobs/583b926fa223ff3d0efb/) Novartis ### [Lead Policy Advocacy Regulatory Affairs and Industry Chambers](https://jobs.opennash.com/companies/accenture/jobs/1adf84698f9dcc805b78/) Accenture ### [Senior Regulatory Affairs Analyst](https://jobs.opennash.com/companies/keurig-dr-pepper/jobs/2db328e46ce9053ed8e1/) Keurig Dr Pepper OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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