Quality Analyst

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:
Quality Systems Analyst

Location:

Boston, MA 02215
Duration: 12 Months Contract

Shift: Monday-Friday (8:00 AM to 5:00 PM) – 40 Hours/Week

(Job Description)

The Position

As a Quality Assurance Associate who will report to the Sr. Director of Quality Assurance Operations, you will be responsible, in partfor assisting with the continued quality oversight of GMP production and testing of clinical trial materials at contract development and manufacturing organizations (CDMOs) and contract testing labs (CTLs). In addition, responsible for review of Regulatory submissions and source data verification The individual will be a collaborative, quality professional with biotech GMP compliance experience, with exceptional communication skills to support a pipeline of gene editing products.

This role will be responsible for document review as well as assisting with the maintenance of phase-appropriate quality systems, including GxP compliance, document control, validation, and quality control. This role is based at Verve's Boston headquarters.

Job Responsibilities

• Assist in Quality oversight for external GMP production and testing activities for clinical stage products and materials
• Review master batch records, executed batch records, analytical testing protocols, methods, reports, testing records, stability documentation, and other quality documentation as needed
• Support the batch disposition process by ensuring that all required documents are accurately and properly completed, including all batch related deviations.

• Perform review of Regulatory submissions and source data verification
  
  Assist in establishing and maintaining internal procedures in compliance with FDA, ICH, EU, and other country-specific regulations
• Other duties as assigned

Qualifications (Required &

Desirable Experience )

• Bachelor's degree (scientific discipline preferred) and 4+ years demonstrated quality experience in GMP environment or pharmaceutical/biopharmaceutical industry
• Strong written and verbal skills
• Ability to communicate across various cross-functional teams
• Ability to work independently and drive pending actions to completion
• Experience in GXP document review
• Strong computer skills – Word, Excel, and other electronic Quality systems

Why Work With Us?
We believe in more than just jobs—we build careers. At Net2

Source, 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
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.

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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