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Quality Control Research Associate - III
Net2Source
- 🇺🇸 United States
- Hybrid
- Manager or above
- 2 days ago
- $50.36 – $53.96 / hour
- JMP
- Minitab
- GLP
- Risk Management
2 days ago
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 theProduct Qualityfunction 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 andinvalid trendingprograms
- Executedata extraction fromLIMs system to support reporting requirements Lead/coordinatecontinuous improvement activitiespartnering with sites.
- Author Annual Product Review Laboratory Section
- Author technical quarterly invalid and biannual controltrending reports
- Interact with the laboratory operations group tosupport new methods, technology, and KLIMS implementationand ongoingsupport for new module implementationsand/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 processesto minimize complexities and optimize operational effectiveness.
- Proficient with statistical tools such asJMP and/or Minitab, Proficient in Microsoft Office application.
- Working knowledge ofquality systems and regulatory requirements (21 CFR Part 11/210/211), Quality Control, GMPs, GLP.
- Master's Degree and4+ 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.
- Experience withgene and cell therapiesor pharmaceutical industry.
- Statistical knowledge in biologics is a plus
- Able to adjust workload based upon changing priorities
- Experience inRisk Management processes a plus
- Experience with US and internationalhealth authority inspectionsa 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
Quality Control Research Associate - III · Net2Source