Validation Engineer, Vacaville

Job Description

Job Description

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.

#TB_PH #ZR

Why TalentBurst? At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth. Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships.We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options. TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce. Company Description Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website



or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX&downtown San Francisco, CA

Company Description

Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada.

We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients.

Please visit our website or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX&downtown San Francisco, CA