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Validation Engineer

Job in Vacaville, Solano County, California, 95688, USA
Listing for: Net2Source (N2S)
Full Time position
Listed on 2026-07-23
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Join a Global Leader in Workforce Solutions – Net2

Source Inc.

Who We Are

Net2

Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price.

Job Title:
Validation Engineer

Duration: 12+ Months (Extendable)

Job Overview

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 Roche/Genentech 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.
  • 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
Our Commitment to Inclusion & Equity

Net2

Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics.

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