Quality Control Research Associate - III

Join a Global Leader in Workforce Solutions - Net2Source Inc.

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 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.

Title- Quality Control Research Associate - III

Location- El Segundo, CA 90245

Duration- 10 months contract

Onsite (initially in Santa Monica for the month of November, some remote time, then return to office in Thousand Oaks)

Number of days per week onsite: 3 "collaboration days" of Tuesday, Wednesday and Thursday

This role will support the Product Quality function reporting to the Director of Analytical Method Lifecycle and Trending but work cross functionally with global and site-based QC SMEs, and other departments within Technical Operations.

Responsibilities (include, but are not limited to):

• Execute global reporting control and invalid trending programs
• Execute data extraction from LIMs system to support reporting requirements Lead/coordinate continuous improvement activities partnering with sites.
• Author Annual Product Review Laboratory Section
• Author technical quarterly invalid and biannual control trending reports
• Interact with the laboratory operations group to support new methods, technology, and KLIMS implementation and ongoing support for new module implementations and/or installation of new capabilities
• Meet reporting deadlines as defined per procedure demonstrating organizational, prioritization, and time management proficiencies
• Highly effective written and oral communication skills to address a cross-functional audience
• Self-motivated, detail-oriented, and willingness to support other team members
• Improve processes to minimize complexities and optimize operational effectiveness.
• Proficient with statistical tools such as JMP and/or Minitab, Proficient in Microsoft Office application.
• Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211), Quality Control, GMPs, GLP.

Basic Qualifications:

• Master's Degree and 4+ years' experience in a Quality function in the pharmaceutical or biotechnology industry
• Bachelor's Degree and 6+ years' experience in a Quality function in the pharmaceutical or biotechnology industry
• High School Degree and 10+ years' experience in a Quality function in the pharmaceutical or biotechnology industry.

Preferred Qualifications:

• Experience with gene and cell therapies or pharmaceutical industry.
• Statistical knowledge in biologics is a plus
• Able to adjust workload based upon changing priorities
• Experience in Risk Management processes a plus
• Experience with US and international health authority inspections a plus.

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