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 requirementsSupport checking for regulatory submissions with Senior RA SpecialistSupport 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