Description
The Validation Engineer I will support and execute QC laboratory equipment qualification activities under direct supervision while complying with cGMP regulations and Roche/Genentech quality standards. Responsibilities include defining qualification requirements, authoring and executing qualification protocols, coordinating with laboratory personnel and vendors, identifying compliance gaps, and supporting continuous improvement. The role is five days onsite in Vacaville, California, Monday through Friday from 8:00 a.m. to 4:00 p.m., and lasts six months.
