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B. Braun

Taipei City Intern Regulatory Affairs

B. Braun

InternshipOn-sitePosted 8 October 2026
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Job description

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Data Privacy Policy Imprint Skip to main content Language Bahasa Melayu ‎(Malay)‎ Bahasa Indonesia ‎(Indonesian)‎ Čeština ‎(Czech)‎ Deutsch ‎(German)‎ English (UK)‎ English ‎(US)‎ Español ‎(Spanish)‎ Français ‎(French)‎ Magyar ‎(Hungarian)‎ Italiano ‎(Italian)‎ 日本語 ‎(Japanese)‎ Polski ‎(Polish)‎ Português ‎(Portuguese)‎ Română ‎(Romanian)‎ Tiếng Việt ‎(Vietnamese)‎ 简体中文 ‎(Simplified Chinese) View Profile Employee Login Language Bahasa Melayu ‎(Malay)‎ Bahasa Indonesia ‎(Indonesian)‎ Čeština ‎(Czech)‎ Deutsch ‎(German)‎ English (UK)‎ English ‎(US)‎ Español ‎(Spanish)‎ Français ‎(French)‎ Magyar ‎(Hungarian)‎ Italiano ‎(Italian)‎ 日本語 ‎(Japanese)‎ Polski ‎(Polish)‎ Português ‎(Portuguese)‎ Română ‎(Romanian)‎ Tiếng Việt ‎(Vietnamese)‎ 简体中文 ‎(Simplified Chinese) View Profile Employee Login Language Bahasa Melayu ‎(Malay)‎ Bahasa Indonesia ‎(Indonesian)‎ Čeština ‎(Czech)‎ Deutsch ‎(German)‎ English (UK)‎ English ‎(US)‎ Español ‎(Spanish)‎ Français ‎(French)‎ Magyar ‎(Hungarian)‎ Italiano ‎(Italian)‎ 日本語 ‎(Japanese)‎ Polski ‎(Polish)‎ Português ‎(Portuguese)‎ Română ‎(Romanian)‎ Tiếng Việt ‎(Vietnamese)‎ 简体中文 ‎(Simplified Chinese) View Profile Employee Login Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Intern - Regulatory Affairs Company: B. Braun Taiwan Co., Ltd. Job Posting Location: Taipei City, Taipei City, Taiwan Functional Area: Regulatory Affairs Working Model: Onsite Requisition ID: 13358 Job Description Administrative and technical documents preparation, data document sorting and archiving, administrative work support. Preparation of License renewal, QSD submissions, Administrative amendments for licenses. Update Chinese IFU to current English IFU by performing gap analysis, translation of contents, and editing Chinese IFU formats per current regulation. Data mapping support to exported data from UDI, SAP, LIS, ALS systems. Update files in license and QSD databases. Filing of Regulation and training presentations. Provide support to RA projects/initiatives. Assist in mastering the progress of MP&A projects. Communications with cross departments within the company and TFDA officers. Ensure all assigned tasks fulfillment within timeline. * The job function listed is not exclusive and shall also include any responsibilities as assigned by the Supervisor from time to time. Qualifications and Requirements Education background in medical or medical device expertise, such as medical science, medicine, nursing or biomedical engineering related field Personal and Skills Good reading and writing skills in Chinese/English Basic data editing and document management ability Good knowledge of MS Word, EXCEL & PowerPoint English IFU reading and translation ability Having relevant experiences in pharma or medical device registration, regulation, etc. are preferred Good concept of human anatomy and physiology, and common disease terms. Careful, detail oriented, Patient Proactive, Can do Attitude Accurate, Independent, Helpful & supportive Apply now Imprint Terms of Use Privacy Policy Cookie Settings Opens in a new tab. Opens in a new tab. Opens in a new tab. Opens in a new tab. Copyright © B. Braun SE Cookie Consent Manager When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. 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