Quality Control Lab Associate Specialist
Durham, North Carolina, United States
Job Description
Join a world-class Quality group dedicated to delivering a safe, compliant, and reliable supply of biopharmaceuticals worldwide. As a Quality Control Lab Associate Specialist, you will play a vital role in product quality assurance by performing microbiological, chemical, and analytical sampling and assays. Working closely with cross-functional teams in Production, Quality Assurance, Validation, and Facilities, you will execute critical environmental and water systems monitoring to support ongoing manufacturing and help bring life-saving medicines to patients.
Responsibilities
Education
Experience
Additional Information
Responsibilities
- Conduct routine environmental monitoring (EM) sampling, including active air, surface, and water systems testing across manufacturing areas.
- Perform in-process and finished product release testing, including sterility testing, residual moisture detection, and average cell dry weight testing.
- Apply aseptic techniques strictly while handling biological samples, evaluating microbiological cultures, and executing assays.
- Adhere strictly to Good Laboratory Practices (GLPs) and current Good Manufacturing Practices (cGMPs) across all lab activities and documentation.
- Collaborate with colleagues to identify and resolve technical or operational shop-floor issues guided by established policies and procedures.
- Evaluate experimental and environmental data, assist with report writing, troubleshoot assays, and participate in process improvement projects.
- Interact cross-functionally with Quality Assurance, Validation, Facilities, and Production teams to support seamless lab and plant operations.
- Maintain clear communication, ask clarifying questions, and ensure alignment with department objectives and next-level management.
Education
- Bachelor's degree in Biology, Microbiology, Biochemistry, or a related scientific field; OR
- Associate's degree in Biology, Microbiology, Biochemistry, or a related field plus 1-2 years of relevant laboratory or pharmaceutical industry experience.
Experience
- Demonstrated understanding and practical application of GLPs, cGMPs, and aseptic technique.
- Hands-on experience performing environmental monitoring and water systems sampling in a regulated environment.
- Proven ability to work effectively within a collaborative, cross-functional team setting.
- Preferred experience utilizing laboratory and production software systems such as LIMS or SAP.
- Preferred strong written and verbal communication skills for data reporting and interdepartmental collaboration.
Additional Information
- Shift Details: 1st Shift Days (Tuesday - Saturday); weekends required.
- Working Hours: 8:30 AM - 5:00 PM (8-hour shift with a 30-minute lunch break), with flexibility for earlier or later start times based on Environmental Monitoring needs.
- Role Impact: Shop-floor decision-making accountability guided by established SOPs and regulatory standards.
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