Pharma QC Analyst - Hybrid (12+ Month Contract)

Pyramid Consulting, Inc; Frederick (MD); Hybrid; USD 80,231,000 - 85,962,000; Full time

Job summary

Pyramid Consulting, Inc. is seeking a Quality Control Analyst (QC Analyst) for a 12+ month contract in Frederick, MD, hybrid. The role involves QC testing of materials and products, plus supporting CoA generation and GMP compliance.

Strong QC, analytical methods, and data integrity experience are required. Responsibilities include method execution (Flow Cytometry, ELISA, qPCR), data trending, deviation investigations, and cross-functional collaboration with Quality, Manufacturing, and Analytical

Qualifications

• Bachelor's or more in a related scientific field with QC experience.
• GMP quality control environment experience required.
• Experience with OOS investigations and root-cause analysis.
• Experience with one or more analytical methods listed (Flow Cytometry, ELISA, qPCR/PCR, cell-based assays).
• Understanding of 21 CFR Part 11/210/211 and data integrity.

Responsibilities

• Perform QC analytical testing on raw materials, intermediates, and products.
• Conduct assays including Flow Cytometry, ELISA, qPCR/PCR, and cell-based methods.
• Review and trend laboratory data; support COA generation.
• Maintain instruments, calibration, maintenance, and troubleshooting.
• Ensure GMP compliance and document laboratory activities accurately.
• Support OOS investigations, deviations, and root-cause analyses.
• Collaborate with Quality, Manufacturing, and Analytical teams.

Education

Bachelor's degree in Biology, Biochemistry, Chemistry, Biotechnology, Microbiology, or related field

Associate's degree + 2 years in biotech QC

High School Diploma/GED + 3 years in biotech QC

Tools

Flow Cytometry

ELISA

qPCR / PCR

Cell-based assays

Laboratory instrumentation calibration

Job description

Pyramid Consulting, Inc. is seeking a Quality Control Analyst (QC Analyst) for a 12+ month contract in Frederick, MD, hybrid. The role involves QC testing of materials and products, plus supporting CoA generation and GMP compliance.

Strong QC, analytical methods, and data integrity experience are required. Responsibilities include method execution (Flow Cytometry, ELISA, qPCR), data trending, deviation investigations, and cross-functional collaboration with Quality, Manufacturing, and Analytical