clia jobs in San Diego

This Bioinformatics Product Owner role focuses on defining and executing the product roadmap for NGS (next-generation sequencing) bioinformatics pipelines and supporting software in precision oncology. The role requires deep domain expertise in cancer genomics, NGS workflows (whole genome, exome, transcriptomics), and clinical genomics standards (FDA, CLIA, CAP, AMP), combined with product management skills to prioritize backlogs, lead Agile ceremonies, and coordinate across bioinformatics, engineering, clinical, and regulatory teams.…See more Key responsibilities include translating clinical and business needs into epics and user stories in JIRA, ensuring FDA compliance and computer system validation (CSV), and optimizing NGS pipeline performance. The ideal candidate brings proven product ownership experience in bioinformatics or oncology software, strong requirement-gathering abilities, and fluency in both technical NGS tools and regulatory frameworks.

This is a senior full-stack engineer role responsible for architecting and building internal platforms and cloud infrastructure that serve operations, finance, lab, and external customers. The engineer will design data models and APIs connecting lab systems, business software (NetSuite, ATS, CRM), and internal dashboards; build robust cloud infrastructure managing provisioning, cost, reliability, and security; and set technical direction on architecture, code quality, CI/CD, and observability across a growing engineering org.…See more The role requires 10+ years of full-stack production experience, deep hands-on cloud infrastructure knowledge, modern frontend (React) and backend skills, and ability to work directly with non-engineering stakeholders to translate ambiguous business requirements into shipped software. Over time, the engineer will build and mentor a team.

The Bioinformatics Test Engineer will design and execute comprehensive testing strategies for NGS (Next Generation Sequencing) data pipelines, including alignment, variant calling, and annotation workflows. Responsibilities include data validation, regression testing, automated test script development in Python, and collaboration with CI/CD pipelines and cloud-based systems.…See more The role requires deep knowledge of NGS file formats (FASTQ, BAM, VCF), proficiency in Python scripting, hands-on experience with Git and CI/CD tools, and familiarity with cloud platforms (AWS/GCP/Azure) to ensure data accuracy and pipeline reliability.

Develop and execute comprehensive automated test plans, test cases, and regression suites for genomics and bioinformatics software applications. Perform functional, integration, regression, and data-validation testing; validate application behavior against genomics concepts (sequencing data, variant calling, sample traceability); and collaborate with wet lab and dry lab teams to translate laboratory workflows into effective test scenarios.…See more Integrate automated tests into CI/CD pipelines, maintain test data, and partner with engineering and product teams on root-cause analysis and quality issue resolution. Requires 3+ years of QA/test automation experience, strong Python skills, hands-on knowledge of genomics fundamentals, and demonstrated experience testing LIMS platforms and life sciences software.

Bioinformatics QA role focused on designing and executing comprehensive testing, validation, and automation strategies for genomics pipelines and laboratory data platforms. Responsibilities include developing automated test suites in Python, validating NGS workflows (FASTQ, BAM, VCF), performing regression and data-validation testing, and collaborating with wet lab and dry lab teams to ensure scientific and technical correctness.…See more The role requires strong Python scripting, CI/CD pipeline experience, cloud platform familiarity (AWS/GCP/Azure), and working knowledge of genomics science fundamentals including sequencing concepts and LIMS integration.

Lead software development for an FDA-cleared blood testing platform, overseeing instrument software, application software, cloud connectivity, cybersecurity, and software quality systems. Manage the full software development lifecycle including requirements, risk management, design controls, verification and validation, and regulatory compliance.…See more Work closely with Quality and Regulatory Affairs on FDA submissions, audits, documentation, and post-market support. Direct strategy, roadmap planning, architecture, and release management for a regulated in vitro diagnostic (IVD) medical device.