Regulatory Affairs Intern - Biomedical Science

What You Will Do

• 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 (i.e. submission dates and approval dates for all medical device listings).

Required Skills and Abilities

• 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 detail. 
• 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.

About Us: 
 
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives.  
 
The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalized healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible.  
 
Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system.  
 
Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management.