Quality Control Chemist I

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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 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 Chemist

Location: Frederick, MD

Duration: 04 months

Shift: Onsite – Shift flexibility preferred (Wed–Saturday, Day or Swing shift)

Note: For the first 7 weeks of the assignment, all contractors are required to work Monday–Friday, 7:30 AM–4:00 PM for New Hire Orientation and Manufacturing Onboarding Technical Training. After completion, candidates will transition to their assigned shift.

Position Summary

The Quality Control Chemist will perform analytical testing and quality control activities in support of biopharmaceutical production. This role requires experience in cell-based assays, molecular biology methods, and GMP laboratory operations. The ideal candidate is detail-oriented, highly organized, and capable of working both independently and collaboratively in a regulated laboratory environment.

Key Responsibilities

• Perform testing of raw materials, intermediates, and final products following established analytical methods including cell-based bioassays, Flow Cytometry, ELISA, and qPCR assays.
• Support routine data trending, record reviews, and ensure accuracy for in-process testing and product release.
• Contribute to Certificate of Analysis (CoA) preparation and data verification for product release.
• Maintain and calibrate laboratory instruments and ensure compliance with GMP requirements.
• Author, review, and revise SOPs, qualification/validation protocols, and technical reports.
• Participate in laboratory investigations and assist in determining root cause for Out of Specification (OOS) results and deviations.
• Monitor and ensure compliance with GMP, SOPs, and company quality systems.
• Review proposed procedural and system changes, ensuring regulatory alignment.
• Gather and report metric information to support continuous improvement initiatives.
• Provide timely updates during daily and weekly team meetings.
• Perform additional duties as assigned.
  
  

Qualifications

Basic Requirements:

• Bachelor's degree in a related scientific discipline
  
  

OR

• Associate degree with 2+ years of experience in biotechnology or Quality Control
  
  

OR

• High School diploma with 3+ years of experience in biotechnology or Quality Control
  
  

Preferred Qualifications:

• Strong knowledge of GMP, SOPs, and quality control processes.
• Experience with OOS investigations and documentation closure.
• Proficiency in MS Word, Excel, PowerPoint, and related tools.
• Excellent written and verbal communication skills.
• Ability to work independently and collaborate effectively with technical personnel.
• Hands-on experience with Flow Cytometry, ELISA, PCR, cell bioassays, and other analytical methods used in biopharmaceutical testing.
• Working knowledge of 21 CFR Parts 11, 210, and 211 regulatory requirements.
• Prior experience in the biotech and/or pharmaceutical industry is highly preferred.
  
  

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.

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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