Voltalabs

Lab Technician- Quality Control

Boston, MA

Lab Technician- Quality Control is an open position at Voltalabs in Boston, MA. Apply directly through the employer below, or browse similar roles.

ABOUT US:

Volta Labs is an applications company that is revolutionizing the future of genomics. We are a Boston based, venture-backed biotech startup that makes extracting vital information from biological samples is as simple as pressing a button, through our flagship product Callisto. Our product speeds up processing time for scientists and increases accessibility to important genetic information for patients. Sitting at the intersection of science and engineering, we invite you to join us on our journey to shape the future of genomics, where insatiable curiosity is encouraged and every Voltarian makes an impact.

THE TEAM:

You'll join a team of innovative thinkers who love to experiment, collaborate, and win together. We are passionate about pushing the boundaries of automation, biology, computing, robotics, design, and user experience to benefit our customers and the world.

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:

Execute PQ and instrument qualification runs per established procedures and acceptance criteria.

Prepare DNA samples, reagents, and consumables for PQ testing.

Perform pre- and post-run QC (DNA concentration, fragment size) using fluorometers, fragment analyzers, thermal cyclers, and centrifuges.

Accurately document run results, QC data, and observations.

Flag unexpected instrument behavior or QC results, and support repeat testing and troubleshooting.

Keep reagents, samples, consumables, and lab inventory organized.

Partner with Quality Assurance and cross-functional teams to ensure consistent PQ execution and complete documentation.

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

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.

Comfortable performing repetitive, detail-oriented lab work with high accuracy.
Strong foundational lab skills: aseptic technique, pipetting, sample dilution, and DNA/reagent handling.
Organized and detail-oriented; follows SOPs and work instructions consistently and keeps accurate records.
Comfortable with lab instruments, software interfaces, and spreadsheets.
Thrives in a fast-paced startup environment with evolving priorities.

Nice to Have

Experience in a GMP/cGMP or other regulated lab, following controlled SOPs and work instructions.
Understanding of Good Documentation Practices (GDP).

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