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, USA and Germany. We are looking for a Regulatory Affairs Specialist who is fluent in English and Chinese (preferable) to help us take care project management related to medical device registrations 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.
