Validation Engineer

This is a contract for six months with possiblity of extension.

Job No. LZAJP00006096

Rate : Up to $60 / hr. on W2 - No 1099 or Corp to Corp

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 policies, procedures and job descriptions.
• Perform any other tasks as requested by Senior Management to support QC laboratory operations.

Job Requirements : Education :

Knowledge / Skills / Competencies :

Work Environment / Physical Demands / Safety Considerations :

Standard office environment