Quality Control Analyst

Contract – 12 Months with a possibility of extension

Shift: Monday – Friday | 8:00 AM – 5:00 PM / 9:00 AM – 6:00 PM

• The QC Analyst supports the Quality Control team in ensuring compliance with established quality processes and standards for manufacturing and production.
• Responsible for performing analytical testing, laboratory support functions, and maintaining quality systems in a cGMP environment.

• Perform routine and non-routine cGMP release and characterization testing using analytical techniques including ddPCR
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• Support laboratory operations by performing assigned testing, documentation, and quality procedures
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• Maintain laboratory standards by ensuring cleanliness, safety compliance, and proper documentation
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• Record and maintain accurate logbooks, equipment usage records, and laboratory documentation
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• Assist in equipment maintenance, calibration, and operational readiness
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• Identify and report deviations; initiate laboratory investigations and quality events with guidance from senior analysts or management.
• Participate in analytical troubleshooting and instrument problem-solving activities
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• Support special projects and assay development activities when required.
• Apply Lean Lab and Six Sigma concepts to improve laboratory processes and efficiency.
• Follow Standard Operating Procedures (SOPs) and update procedures when necessary.
• Collaborate with team members to ensure quality, accuracy, and timely completion of tasks
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• Perform other related duties as assigned
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• Bachelor’s degree in Biochemistry, Biology, Microbiology, or a related scientific discipline
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• Basic understanding of laboratory testing and analytical techniques
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• Ability to apply company policies and procedures to resolve routine issues.
• Strong attention to detail and organizational skills
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• Ability to work effectively in a team environment
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• Good written and verbal communication skills
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• Ability to follow detailed instructions and standard laboratory procedures
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