Validation Engineer
Listed on 2026-07-23
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
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 OverviewSchedule:
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.
- 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
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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