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 an…
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 an…
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Full-time
bachelor degree
Posted 50d ago
~40 hrs/week
Responsibilities
Responsible for managing product registration and approval applications to minimize timelines and ensure regulatory compliance. This includes coordinating with head offices and factories, managing submission data, and maintaining relationships with regulatory authorities and KOLs.
Requirements
Requires a Bachelor's degree or higher in medicine or pharmacy with over 7 years of relevant work experience. Candidates must be familiar with drug administration laws and possess strong communication, leadership, and language skills in English or Japanese.
Full 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.
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society.
We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities.
Read our community guidelines: https://takeda.info/communityguidelines
Offices: Tokyo, JP · 1 Takeda Parkway, Deerfield, Illinois 60015, US · 40 Landsdowne St, Cambridge, Massachusetts 02139, US · Avenida das Nações Unidas, 14.401, Torre Jequitibá - 10°, 11° e 12° andares, São Paulo, 04794-000, BR · 43 Old Oak Rd, Bellville, Western Cape 7550, ZA
How many Healthcare jobs are open in Beijing, China right now?
There are currently 544 open healthcare positions in Beijing, China listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Beijing, China?
Companies currently hiring include Sanofi, IQVIA, Takeda, GE HealthCare, ICON plc, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Beijing, China?
Yes — 108 of the 544 open healthcare positions offer remote or hybrid work (33 remote, 75 hybrid).
How do I apply for Healthcare jobs in Beijing, China?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.