Validation Engineer - Contract

Position: Validation Engineer I,Req#: LZAJP00006878

Location: Vacaville, CA (100% onsite)
Duration: 6+ Months Contract with the possibility of extension

M-F 8 am - 4 pm, 5x onsite

Job Description:

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

Education and Experience:

• BS/BA degree (preferably in a relevant scientific discipline)
• Minimum of two years’ experience in Validation or equipment qualification is desired.
• Experience (may vary depending on site size/scope)
• Experience in the pharmaceutical, biopharmaceutical industry or an equivalent combination of education and experience.
• Knowledge of cGMP or equivalent regulations.
• Ability to make sound decisions about scheduling and managing priorities.
• Flexibility in problem solving, providing direction and work hours to meet business objectives.

Knowledge/Skills/Competencies:

• Possesses strong verbal and written communication skills and the ability to influence at all levels
• Capable of building trustful and effective relationships
• Able to think strategically and translate strategies into actionable plans
• Takes responsibility, drives results, and achieves expected outcomes

Work Environment/Physical Demands/Safety Considerations:

• Standard office environment

Job Responsibilities: 

• 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.