About this Lab Technician- Quality Control role at Voltalabs
THE ROLE
Volta Labs is seeking a hands-on Quality Control Laboratory Technician to support Performance Qualification (PQ), quality control, and validation for the Callisto digital fluidics automation platform. You'll run standardized genomics sample prep workflows, perform post-run QC, and document results that confirm Callisto systems and protocols perform reliably across repeated runs.
This is an execution-focused bench role, ideal for someone early in their career who enjoys following detailed procedures and building strong lab practices. You'll be trained on Callisto workflows, QC methods, and PQ procedures, and grow toward independence on routine work.
You'll report to the Scientific Program Manager and work closely with Quality Assurance, Application Development, and Instrument Manufacturing.
DAY 1 TO YEAR 1:
Within 3 months you'll…
Learn Callisto basics, PQ workflows, SOPs, acceptance criteria, and documentation standards. Become proficient in sample, reagent, and instrument prep and routine QC (Qubit, fragment analysis), and begin executing PQ runs under guidance.
Within 6 months you'll…
Independently run Callisto PQ workflows end-to-end, from preparation through post-run QC and documentation. Flag deviations in QC metrics, instrument behavior, or workflow execution, and assist with repeat testing and troubleshooting.
Within 12 months you'll…
Serve as a dependable execution lead for routine PQ activities, escalating deviations and instrument concerns appropriately. Provide data and observations that support root-cause investigations, train new technicians, and identify ways to improve PQ efficiency and documentation.
WHO YOU ARE
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Associate's degree with 1–2+ years of industry wet lab experience; Bachelor's in Biology, Molecular Biology, or equivalent with 0–2 years of wet lab experience (industry, academia, or internship) preferred.
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Comfortable performing repetitive, detail-oriented lab work with high accuracy.
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Strong foundational lab skills: aseptic technique, pipetting, sample dilution, and DNA/reagent handling.
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Organized and detail-oriented; follows SOPs and work instructions consistently and keeps accurate records.
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Comfortable with lab instruments, software interfaces, and spreadsheets.
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Thrives in a fast-paced startup environment with evolving priorities.
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Experience in a GMP/cGMP or other regulated lab, following controlled SOPs and work instructions.
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Understanding of Good Documentation Practices (GDP).
Nice to Have
