- Reporting to the Regional Regulatory Affairs Manager, Southeast Asia, the Regulatory Affairs Intern is responsible for:
- Archive and maintain regulatory files in a format consistent with local health authority and company requirements
- Support checking for regulatory submissions with Senior RA Specialist
- Support Senior RA Specialist on the admin tasks of Regulatory Affairs function, including but not limited to payment request, send out document(s) for translation and notarization, etc.
- Support to obtain and manage permits and licenses for the importation of products from different Local Government Agencies.
- Support to review and submit advertisement materials of related BUs if appropriate.
- Support to promote awareness and train the local team to maintain compliance.
- Prepare, order and maintain documents for tender. Coordinate to provide documents for customer concerns.
Education / Professional Certification
- Final year students in university of Pharmacy or Life Sciences, i.e. Biomedical, Biochemistry, Pharmaceutical Studies or Medical Engineering, or equivalent.
Experience
- Not required.
Knowledge / Skills / Other characteristics
- Proficiency in Basic Microsoft Word, PowerPoint and Excel
- Proficiency in English both written and spoken
- Communication skill & Interpersonal skill
- Meticulous and detail orientated
- Positive working attitude with passion to learn and develop.
Your ZEISS Recruiting Team:
Doan Le Thuy Duong
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