Regulatory Affairs Lead IVD & 510K Specialist (Mandarin)

A global biotechnology company in San Diego is seeking a Regulatory Specialist with expertise in IVD products and 510(k) submission processes. The role involves preparing regulatory applications, managing compliance with FDA regulations, and providing guidance on product development projects. Candidates should have a Bachelor's degree in Life Sciences and a minimum of 5 years of relevant industry experience, including proficiency in Mandarin. The position offers benefits such as a health care plan and 401K. #J-18808-Ljbffr