Let’s talk about the team:

The Regulatory Affairs team dedicated to provide support and guidance with respect to regulatory environment, at all stages of the life cycle of ResMed's products. Ensuring compliance and delivery of optimal regulatory strategies for portfolio planning, active regulatory intelligence and excellence in execution. You will work closely with all internal stakeholders and external regulators to achieve business goals.

Let’s talk about the role:

Support responsible RA to prepare the NMPA/MIIT Submission dossierEnsure products are registered according to plans; oversee product registrations and maintain appropriate records for product compliance bodiesEnsure that necessary licenses and certifications are kept updated and renewed as applicable.Secure compliance of products and services distributed, including import-export & transportation (regulations related to customs things, labeling and shipping, et al) .Ensure the timely delivery of new regulations or regulatory environment in China, offer necessary analysis.Ensure smooth and efficient communication with global team and local commercial team.

Let’s talk about you:

Bachelor’s degree.Minimum of 1 years of related experience in international company or 2-3 years in local company, medical device field is preferential.Good oral/written EnglishGood communication skill;Team work spirit, work passion and positive work attitude.

Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now!