Clinical Laboratory Scientist, (Technical Supervisor)

Benefits

Parental leave

Not verified

Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

Not verified checked Jun 13, 2026

Salary

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401(k) match

Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)

$111,944 U.S. median for this role

Projected growth (BLS Employment Projections)

+13.7% - Much faster than average

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type

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Weekend work

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Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Clinical Laboratory Scientist, (Technical Supervisor) Pleasanton, California, USA HQ About The Role: 10x Genomics is establishing a diagnostics effort to translate our leading single-cell and spatial genomics technologies into impactful clinical applications. This Clinical Laboratory Scientist/Technical Supervisor position performs and provides scientific and technical oversight for high complexity next-generation sequencing (NGS) assays within a CLIA-certified laboratory. This role is accountable for ensuring the operational execution, analytical validity, performance, and regulatory compliance of all NGS testing. The Technical Supervisor serves as the subject matter expert for assay validation, quality systems, and troubleshooting, and partners closely with laboratory leadership to maintain operational excellence and continuous improvement. What You Will Be Doing: Provide operational execution and technical oversight of high complexity NGS assays, ensuring analytical accuracy and reliability of test results. Validate, and implement NGS assays in accordance with CLIA, CAP, and applicable regulatory standards. Establish and monitor quality control (QC) and quality assurance (QA) programs, including review of performance metrics, trends, and corrective actions. Author, review, and approve technical documentation, including standard operating procedures (SOPs), validation protocols/reports, and test methods. Ensure compliance with all regulatory requirements and support internal and external audits and inspections. Serve as the primary technical resource for troubleshooting complex assay, instrumentation, and bioinformatics issues. Evaluate and approve changes to assays, workflows, instrumentation, and software, including revalidation as required. Oversee proficiency testing, method comparisons, and ongoing assay performance monitoring. Provide technical training and competency assessment for laboratory personnel. Collaborate with cross-functional teams (bioinformatics, R&D, quality, and operations) to support

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