You will lead medical device regulatory affairs activities in China for Apple Health. You will demonstrate the ability to develop a variety of solutions to RA/QA challenges and will exercise independent judgment in settling and communicating appropriate regulator action and engagement strategy. Key responsibilities include:- Develop and execute clear regulatory strategies for Apple Health features in China.- Communicate and align regulatory plans with internal Apple teams.- Lead regulatory authority discussions.- Monitor and assess regulation changes and partner with other Apple teams to shape regulations and guidances as necessary.
Bachelors degree or equivalent in science or engineering.
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