What are the responsibilities and job description for the QC Analyst I position at Net2Source (N2S)?
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Who We Are
Net2Source 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 32 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 Description:
Job Title: QC Associate I
Location: Vacaville, CA 95688
Duration: 07 Months (Extendable)
Pay Rate: $25.00 - 27.93/hr on W2
Summary
With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.
Job Responsibilities
- Perform a broad variety of basic and moderately complex tests with documentation according to GMP
- Review data and assess against established acceptance criteria
- Perform technical review of peer-generated data
- Evaluate data to identify trends and/or establish limits
- Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
- Identify and troubleshoot technical problems
- Identify gaps in systems and procedures
- Receive and provide training
- Participate in assay transfer and assay validation
- Perform equipment qualification / maintenance
- Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures
- Support the maintenance and compliance of operational areas
- Assure and apply GMP throughout operations
- Coordinate with customers to support multi-site operational activities
- Support internal and external audits and regulatory inspections
- Works to meet schedules, timelines, deadlines
- Participate in and/or lead group and project teamwork; project and process improvements
- Write protocols and reports under limited supervision
- Meets scheduled performance of 95% on time
- Perform other duties as requested by managers to support Quality activities
Job Requirements
- B.S./B.A. degree and 1-3 years experience or Master’s Degree plus one year experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
- Strong verbal and written communication skills, ability to organize and present information both formally and informally.
- Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
- Routinely exercises sound judgment, reasoning and problem solving.
- Capable of working under limited supervision and determining own short term priorities.
Why Work With Us?
We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter.
Our Commitment to Inclusion & Equity
Net2Source 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.
Awards & Recognition
- America’s Most Honored Businesses (Top 10%)
- Fastest-Growing Staffing Firm by Staffing Industry Analysts
- INC 5000 List for Eight Consecutive Years
- Top 100 by Dallas Business Journal
- Spirit of Alliance Award by Agile1
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Salary : $17 - $28