Lab Technician- Quality Control

Lab Technician- Quality Control

Seaport District, Boston, MA

Application Development /

Full-time /

On-site

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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).

$55,000 - $65,000 a year

Our Benefits and Perks:

• Robust Equity Program, to build future wealth through stock options with high growth potential
• Comprehensive Healthcare Coverage, including Medical, Dental, & Vision
• HSA with monthly company contribution, & FSA
• Sponsored Commuter Benefit Plans
• Access to Our 401K Plan, to save for your future
• 12 Weeks of Paid Parental Leave
• Paid Time Off, because we understand the importance of time off for rest and adventure
• 11 Paid Holidays
• Twice Weekly Company Lunches, office snacks, beverages, & treats
• Monthly Team Happy Hours and regular team outings!

We are an equal opportunity employer and foster diversity and inclusion at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status, and we actively seek out and value diverse backgrounds and experiences.

Even if you don''t check every box, but see yourself positively contributing, please apply. Help us build an inclusive community that will change the face of genomics!

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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