Quality Control Chemist I

Job Description

Job Description

Job Description: Quality Control Chemist I
Location: 9021 Bennett Creek Blvd, Frederick, MD 21704
Pay Rate: $29/hr Bill Rate
Shift: Wednesday–Saturday, 3:00 PM – 1:30 AM EST

Training Schedule

For 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 completing training, the contractor will move to the agreed-upon shift.

Job Summary

The Quality Control Chemist I will perform laboratory testing of raw materials, intermediates, and finished products in a regulated biopharmaceutical environment. The position supports product release, laboratory operations, quality documentation, equipment maintenance, and GMP compliance.

Key Responsibilities

• Perform testing of raw materials, intermediates, and final products.
• Conduct analytical testing using cell-based bioassays, flow cytometry, ELISA, and qPCR assays.
• Maintain laboratory equipment and perform routine calibration and maintenance.
• Monitor and trend laboratory data and review test records.
• Support in-process, drug substance, and drug product release testing.
• Provide information to support the generation of Certificates of Analysis (CoAs).
• Author and revise SOPs, qualification protocols, validation protocols, and reports.
• Assist with Out-of-Specification (OOS) investigations and root-cause analysis for deviations.
• Participate in daily and weekly meetings and provide status updates.
• Ensure compliance with GMP systems and documented procedures.
• Support continuous improvement initiatives and other assigned duties.

Basic Qualifications

Candidates must meet one of the following:

• Bachelor's degree; OR
• Associate's degree with 2+ years of biotechnology or related-field experience and Quality Control experience; OR
• High school diploma with 3+ years of biotechnology or related-field experience and Quality Control experience.

Preferred Qualifications

• Strong knowledge of GMP, SOPs, and Quality Control processes.
• Experience identifying, writing, evaluating, and closing OOS investigations.
• Proficiency in Microsoft Word, Excel, PowerPoint, and other applications.
• Strong written and verbal communication skills.
• Ability to work independently and communicate with scientific and technical personnel.
• Experience with analytical techniques such as:
• • Flow Cytometry
  • ELISA
  • PCR / qPCR
  • Cell-Based Bioassays
• Working knowledge of quality systems and regulatory requirements, including 21 CFR Part 11, 210, and 211.
• Previous pharmaceutical or biotechnology industry experience.

\nCompany 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.

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.