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Validation Engineer

eTeam Inc.

  • Vacaville, CA
  • 22 days ago

    Highlights

    Experience (may vary depending on site size/scope) Experience in the pharmaceutical/biopharmaceutical industry, or an equivalent combination of education and experience. Maintains the company’s right to operate, supply to patients, and cost-effectiveness by actively participating in continuous improvement projects.
    eTeam Inc.

    Numbers & Facts

    LocationVacaville, CA
    IndustryOther/Not Classified
    Company Size100 to 499 employees
    Year Founded1998
    Websitewww.eteaminc.com

    Description

    Job Title: Validation Engineer
    Location: Vacaville, CA
    Duration: 12 Months

    Job Description:

    Schedule: Monday – Friday, 8:00 AM – 4:00 PM (includes a 30-minute unpaid lunch)

    Location: 100% Onsite (5x/week)

    Job Summary
    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 corporate principles, 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.

    Duties

    <,>Technical 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.

      Job Requirements

      Education
      BS/BA degree (preferably in a relevant scientific discipline)

    <,>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.
      Minimum of two years’ experience in Validation or equipment qualification is desired.
      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

       

    About Company

    Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.

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