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Senior Manager, RA, GI&I

Takeda


Job Location:

Beijing - China

Monthly Salary: Not provided by the employer
Posted: 3 July 2026 (30+ days ago)
Application Deadline: 30 September 2026
Vacancies: 1 Vacancy

Job Summary

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Job Description

Accountabilities:

In accordance with the companys product launch strategy and departments 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:Bachelors 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

Required Experience:

Senior Manager


About Company

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Takeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.

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