Quality Control Chemist | Frederick, MD | Pay Rate: 30$/hr. On W2

Job Description

Job Description

Job Title: Quality Control Chemist

Location: 9021 Bennett Creek Blvd, Frederick, MD 21704 (Onsite)

Duration: 06+ Month Contract

Working Model: Fully onsite

Schedule: Wednesday–Saturday, 3:00 PM–1:30 AM after training

Pay Rate: 30$/hr. On W2

Schedule Note: The role is fully onsite. During the first 7 weeks, contractors must work Monday–Friday, 7:30 AM–4:00 PM for New Hire Orientation and Manufacturing Onboarding Technical Training. After training, the contractor moves to the agreed Wednesday–Saturday, 3:00 PM–1:30 AM shift.

Job Description

We are seeking a Quality Control Chemist I to support quality control testing and GMP operations at a biopharmaceutical manufacturing site in Frederick, MD.

Key Responsibilities:

• Perform testing of raw materials, intermediates, and final products using analytical methods including:
• • Flow Cytometry
  • ELISA
  • qPCR/PCR
  • Cell-based bioassays
• Maintain laboratory equipment and perform routine calibration and maintenance.
• Monitor and trend analytical data and perform routine review of test results and documentation.
• Support in-process testing, drug substance, and drug product release activities.
• Provide information supporting generation of Certificates of Analysis (CoAs).
• Assist with OOS investigations, deviations, and root-cause analysis related to analytical procedures.
• Author or revise SOPs, qualification/validation protocols, and reports.
• Ensure laboratory activities comply with established GMP procedures and quality systems.
• Participate in daily/weekly team meetings and continuous improvement activities.
• Work with internal and external resources to maintain the laboratory in an optimal condition.

Basic Qualifications

• Bachelor’s degree, OR
• Associate/AA degree with 2+ years of biotechnology or related experience plus Quality Control experience, OR
• High school diploma with 3+ years of biotechnology or related experience plus Quality Control experience.

Preferred Qualifications

• Strong understanding of GMP, SOPs, and Quality Control processes.
• Experience with OOS investigations, deviations, and root-cause analysis.
• Hands-on experience with Flow Cytometry, ELISA, PCR/qPCR, and cell-based assays.
• Knowledge of 21 CFR Part 11, 210, and 211.
• Experience in the biotechnology/pharmaceutical industry.
• Strong documentation, communication, and collaboration skills.
• Proficiency with MS Word, Excel, and PowerPoint.

LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Company Description

LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.