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About the Role
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. The ideal candidate has hands-on experience with molecular biology and NGS technologies and is passionate about developing innovative diagnostics in a collaborative, fast-paced product development environment.
Responsibilities
- Support the development, optimization, verification, and transfer of NGS-based MRD assays 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.
- Generate high-quality laboratory data and maintain accurate documentation.
- Contribute to SOPs, protocols, reports, and other development documentation.
- 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.
- Support technology transfer, assay implementation, and validation activities within the clinical laboratory environment.
Requirements
- Strong molecular biologist with hands-on experience in NGS workflows and common NGS quality control methods.
- 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.
Skills
- Molecular Biology
- NGS Workflows
- NGS Quality Control Methods
- Tapestation/Fragment Analysis
- Fluorescence-based Quantification
- qPCR
- Biochemistry
- Genetics
- Experimental Design
- Troubleshooting
- Assay Optimization
- Data Analysis
- Statistical Analysis
- Data Visualization
- JMP
- R
- Python
- Oncology
- Liquid Biopsy
- ctDNA
- MRD Technologies
Location
- Onsite
Work Type
- Full-time
Experience Level
- Scientist I
- Minimum of 3 years of relevant industry and/or postdoctoral experience
Education Level
- Ph.D. in Molecular Biology, Genetics, Biochemistry, Cancer Biology, or a related field.
Salary/Compensations
- $130,000—$140,000 USD
Benefits
- Competitive compensation and benefits
- Significant career opportunities
- Eligible for additional discretionary bonuses/incentives
- Eligible for restricted stock units
About the Company
- Veracyte is a global diagnostics company whose vision is to transform cancer care for patients all over the world.
- We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer.
- Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine.
- Recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel.
Equal Opportunity
- Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status.
- Veracyte participates in E-Verify in the United States.