San Diego, California
•
Today
5 to 6 years of medical devices or diagnostic equipment manufacturing experienceManage the end-to-end validation documentation lifecycle including authoring, reviewing and approving protocols (URS, IQ, OQ, PQ, PV, TMV, RTM, VSR) Change Controls and Periodic Reviews, ensuring alignment with site VMP and ISO 13485.Lead cross-functional validation initiatives for lab equipment, facilities, and non-product software supporting diagnostics platformsQualify GXP equipment in compliance with FDA 21 CFR P
Easy Apply
Contract
Depends on Experience


















