Validation Engineer I

M-F 8am - 4pm (including unpaid lunch 30 mins) 5x onsite

Job Summary:
With direct supervision, candidate is responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Roche/Genentech corporate principals, quality policies, standards and core values. Maintains company s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects.

Duties:
Technical:
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.
Identify business, quality, and compliance gaps.
Sign documents for activities as authorized and described by Genentech polici...

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