Job Title: CAPA Coordinator
Location: Foster City, CA (2-3 days onsite)
Duration: 12 Months
Interview: Video

CAPA authoring/Planning
CAPA Project Mgmt
Investigation experience
Managing Quality Events
Deep understanding of QMS
Deviation investigations, Product Complaints, Audit Observations, SOP authoring, maybe Doc Control, etc.
Knowledge in Clinical, Product Dev, Manufacturing, Supply Chain, Facilities, and Analytical functional areas.