QA Shop Floor Analyst - 3rd shift

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: QA Shop Floor Specialist
Duration: 12 Months (Contract)
Location: Fort Washington, PA

Shift:
• Option 1: Sunday - Wednesday, 9:30 PM - 8:00 AM EST
• Option 2: Wednesday - Saturday, 9:30 PM - 8:00 AM EST
(4 x 10-hour shifts per week)

Position Summary
• Provide daily Quality Assurance (QA) support on the manufacturing floor to ensure compliance with internal procedures, cGMP, and CFR regulations
• Interact with cross-functional teams including Manufacturing, Packaging, Quality Laboratories, Validation, Engineering, Maintenance, and other site departments
• Support critical quality functions such as Batch Record Review, Product Release, SOP compliance, Investigations, CAPA, Change Control, and Shop Floor Audits

Key Responsibilities
• Deliver daily QA support to warehouse, bulk manufacturing, and packaging operations
• Communicate quality events promptly to management and maintain proper documentation
• Perform or support Batch Record Review, Raw Material, Bulk, and Finished Product Releases
• Conduct and support investigations (including writing, reviewing, and approvals)
• Perform Line Audits and Cleaning Verification activities to ensure compliance
• Support the design, creation, and revision of SOPs, quality processes, and training initiatives
• Assist in Consumer Complaint investigations and related documentation
• Collaborate with project teams, providing QA expertise where required
• Capture and analyze site quality metrics, recommending process improvements
• Train new employees and represent QA positively in cross-functional settings
• Proactively identify and report deviations, ensuring timely resolution

Qualifications
• 3 years of experience in Quality Assurance within a GMP-regulated pharmaceutical or manufacturing environment
• Strong knowledge of cGMP, CFR, and FDA regulations
• Hands-on experience with Batch Record Review, Product Release, CAPA, and Change Control
• Excellent communication skills and ability to interact with cross-functional teams
• Strong problem-solving skills and ability to manage multiple priorities under limited supervision
• Familiarity with documentation systems and quality management tools

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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