Validation Engineer
📋 Role Overview & Responsibilities
Location: 100% onsite in Vacaville, CAType: 8 month contract Pay: $59 - $77 per hour (depending on experience)
MUST HAVE: 3- 6 years of experience working in a cGMP environment.
Primarily responsible for the support and execution of laboratory equipment qualification and associated computer system validation activities in compliance with current cGMP regulations and corporate principles, quality policies, standards, and core values. You will work closely with instrument vendors, facilities, IT and lab personnel to coordinate the, installation and the qualification including computer system validation, of QC Equipment.Reader.
Perform qualification of laboratory equipment in accordance with EQ policies, plans and procedures.Coordinate with laboratory personnel to define qualification requirements.Author, review and execute equipment qualification protocols.Coordinate equipment qualification activities with vendors and other support groups.Coordinate equipment maintenance activities with vendors and other support groups, as required.Identify business, quality, and compliance gaps and propose and implement potential improvements to systems and proceduresSign documents for activities as authorized and described by Genentech policies, procedures and job descriptions.Provide input to technical / investigation reports.Identify, troubleshoot, and propose resolution to technical problems.Receive and provide training.Provide input to and participate in assay transfer/validation associated with equipment qualification/lifecycle.Coordinate with customers to support multi-site operational activities.Present equipment lifecycle and associated procedures/material during internal and external audits and regulatory inspections.Works to meet schedules and set timelines.Perform other duties as requested by managers to support Quality acti
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