Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.

Main Responsibilities:
Manage regulatory submission and approval in cooperation with local and global teams to ensure our products are listed in a timely manner and business objectives are met
Submit technical documentation to the Department of Health for new/change listing application of medical devices
Maintain Regulatory Affairs (RA) database and provide local and global RA teams with real-time information required to maintain key metrics 

Requirements: 
Have knowledge in Biomedical Science, Biochemistry, Biology or Science-related field
Good analytical, interpersonal communication and problem-solving skills
Self-starter, highly motivated with attention to details
Be able to work independently, by taking general concepts and direction to produce desirable compliant outcomes.
Excellent command of written and spoken English and Chinese

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an Equal Opportunity Employer.