Quality Control Chemist

Net2Source (N2S); Frederick (MD); On-site; USD 34,000 - 62,000; Full time

Job summary

Net2Source Inc. is seeking a Quality Control Chemist for a 12-month contract onsite.

The role requires performing testing of raw materials, intermediates and final products using analytical methods and QC procedures while maintaining laboratory equipment and ensuring compliant documentation for release. The candidate should have a degree in biotechnology or a related field with QC experience, knowledge of GMP and SOPs, and experience with analytical techniques such as flow cytometry, ELISA, and

Qualifications

• Bachelor's Degree or AA Degree with 2+ years' biotechnology or related field and Quality Control experience, OR High School Degree with 3+ years' biotechnology or related field and Quality Control experience.
• Requires hands-on QC experience in biotechnology or related field.
• Knowledge of GMP, SOPs and quality control processes.

Responsibilities

• Perform testing of raw materials, intermediates and final products by following analytical methods including flow cytometry, ELISA and qPCR assays.
• Maintain lab in optimal state and manage instrument calibration and routine maintenance.
• Assist with monitoring and trending data, review routine test data and related documents for in-process testing, drug substance and drug product release; generate CoAs for product release.

Skills

Quality control

Communication skills

Independent work

Education

Bachelor's/AA with QC experience

HS diploma with QC experience

Tools

MS Word

Excel

PowerPoint

Job description

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 Chemist

Duration- 12 months contract

Onsite - Shift flexibility preferred

Responsibilities (include but are not limited to):

• Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
• Work with internal and external resources to maintain lab in an optimal state.
• Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. Supply information to support generation of CoAs for product release.
• Maintains laboratory instruments for calibration and routine maintenance
• Author or revise SOPs, qualification/validation protocols and reports.
• Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.
• Provide updates at daily and weekly meetings.
• Monitor the GMP systems currently in place to ensure compliance with documented policies.
• Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.
• Gather metric information for use in continuous improvement of areas of responsibility.
• Perform other duties as required.

Basic Qualifications:

• Bachelor's Degree OR AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience OR High School Degree and 3+ years' experience in biotechnology or related field and Quality Control experience

Preferred Qualifications:

• Strong knowledge of GMP, SOPs and quality control processes.
• Identifying, writing, evaluating, and closing OOS's and investigations.
• Proficient in MS Word, Excel, Power Point and other applications.
• Strong written and verbal communication skills.
• Ability to communicate and work independently with scientific/technical personnel.
• Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
• Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
• Preferred: Experience in the biotech and/or pharmaceutical industry.

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