# Scientist I

**Company**: Veracyte
**Location**: South San Francisco, California
**Work arrangement**: onsite
**Experience**: senior
**Job type**: full-time
**Salary**: $130,000-$140,000 USD
**Category**: Research
**Industry**: Healthcare

**Apply**: https://job-boards.greenhouse.io/veracyte/jobs/5207342007?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_96cf4d5a-e6f

## Description

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe.

We are seeking a highly motivated Scientist I to support the development of next-generation MRD assays from concept through clinical laboratory implementation. This laboratory-based individual contributor will execute and analyze experimental studies supporting assay development, workflow optimization, automation, and validation readiness.

## Responsibilities:

- Support the development, optimization, verification, and transfer of NGS-based MRD assays under the guidance of senior technical team members from early feasibility through clinical laboratory implementation.

- Execute feasibility, characterization, optimization, and pre-validation studies to support assay and workflow development.

- Procure, qualify, prepare, and characterize clinical and contrived samples for assay development and validation studies.

- Contribute to experimental design, study planning, execution, analysis, and interpretation in collaboration with senior scientists and technical leads.

- Generate high-quality laboratory data and maintain accurate documentation in accordance with design control and quality system requirements.

- Contribute to SOPs, protocols, reports, and other development documentation supporting product development activities.

- Support development and optimization of automated high-throughput laboratory workflows.

- Participate in assay troubleshooting, root-cause investigations, and implementation of technical improvements.

- Collaborate with cross-functional teams including Bioinformatics, Data Science, Operations, Clinical Laboratory, Automation, Quality, Regulatory, and Software/LIMS to advance product development objectives.

- Support technology transfer, assay implementation, and validation activities within the clinical laboratory environment.

## Who You Are:

- Strong molecular biologist with hands-on experience in NGS workflows and common NGS quality control methods, such as Tapestation/fragment analysis, fluorescence-based quantification, and qPCR.

- Laboratory scientist who enjoys bench experimentation and can independently execute laboratory activities with a high degree of rigor and attention to detail.

- Skilled in applying molecular biology, biochemistry, and genetics principles to experimental design, troubleshooting, and assay optimization.

- Effective problem solver with demonstrated ability to troubleshoot and optimize molecular biology workflows.

- Data-driven scientist capable of analyzing experimental results and communicating findings clearly and effectively.

- Organized and detail-oriented contributor who can manage multiple projects and priorities in a dynamic environment.

- Strong collaborator who works effectively across multidisciplinary teams and functions.

- Clear and effective communicator with strong written and verbal communication skills.

- Flexible and open-minded contributor who adapts well to changing priorities and business needs.

- Passionate about developing diagnostic products that improve outcomes for cancer patients.

## Qualifications:

- Ph.D. in Molecular Biology, Genetics, Biochemistry, Cancer Biology, or a related field.

- Minimum of 3 years of relevant industry and/or postdoctoral experience in molecular diagnostics, biotechnology, genomics, or a related field.

- Hands-on experience with NGS-based molecular biology techniques including library preparation and supporting analytical methods.

- Strong understanding of molecular genomic technologies, including DNA- and/or RNA-based assays.

- Experience with experimental design, execution, data analysis, and interpretation.

- Familiarity with statistical analysis and data visualization tools such as JMP, R, Python, or equivalent.

- Experience working with clinical sample types, including blood, plasma, tissue, or FFPE specimens, is preferred.

- Exposure to regulated product development environments and quality systems (CAP/CLIA, NYSDOH, design control) is desirable.

- Experience with oncology, liquid biopsy, ctDNA, or MRD technologies is a plus.

## What We Can Offer You

Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions.

## Skills

### Required
- Molecular Biology
- NGS workflows
- biochemistry
- genetics
- experimental design
- data analysis
- troubleshooting

### Nice to have
- oncology
- liquid biopsy
- ctDNA
- MRD technologies
- statistical analysis
- data visualization tools

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Source: [Apply at job-boards.greenhouse.io](https://job-boards.greenhouse.io/veracyte/jobs/5207342007?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)