WHO ARE WE?
UIH is a leading global medical device developer and supplier with a diversified portfolio of advanced imaging equipment and healthcare IT solutions. We are building an innovative team with the mission of developing and supplying advanced technologies and improving patient care worldwide. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
The Regulatory Affairs Specialist will be responsible for establishing best practices in the area of pre- and post-market regulations, submissions and new product development.
This position will require international travel and training for 2 weeks in Shanghai, China.
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