Summary of Responsibilities:

Develop and optimize the vigilance system to ensure product vigilance activities fully align with Chinese regulatory requirements and B.Braun Global’s standards.
Manage and maintain vigilance data on regulatory product vigilance monitoring platforms system and perform necessary risk assessments.
Lead the development and capacity building of the PV (pharmacovigilance and medical device) team, driving team effectiveness and expertise enhancement.

Education and Qualificaitons:

Bachelor degree or above, major in Clinical Medical/Clinical Medicine/Epidemiology related
Fluent in English speaking and writing.
At least 10 years total working years with minimum 5 years in medical device & pharmaceutical vigilance area, clinial experience is preferred, and 2 years of experience in people manager role.