Thực tập sinh Đăng ký sản phẩm ( Regulatory Affairs Intern)

Introduction
Qualtech is an Asia Medical Device Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand, Korea, USA and Germany. We are looking for a Talented Regulatory Affairs Intern who is fluent in English and be able to understand to medical device regulations in the countries we service for. Qualtech is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people.
Job description
Oversight of regulatory submissions for assigned projects/countries, which may include completion of submissions or notifications, as required.
Ability to read and understand regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
Investigating proactively and capitalizing regulatory information collected throughout studies and maintain Regulatory database accordingly.
Other duties as assigned.