Veracyte is a genomic diagnostics company that develops molecular tests to help clinicians diagnose and guide treatment for cancer patients. Its test menu covers thyroid, prostate, bladder, breast, and lung cancers, using genomic classifiers such as Afirma and Decipher. The company operates high-complexity clinical laboratories and is publicly traded on the Nasdaq Global Market.

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. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values:<ul><li>We Seek A Better Way: We pursue bold ideas, embrace complexity, and keep pushing forward.</li><li>We Make It Happen: We act with urgency, deliver with excellence, and always find a way. </li><li>We Are Stronger Together: We engage with empathy, align around what's best for Veracyte, and celebrate as one team. </li><li>We Care Deeply: We show up with integrity, kindness, and respect for one another. </li></ul><h3>The Position:</h3>We are seeking an experienced and motivated Bioinformatics Scientist to join our Bioinformatics and Data Science Team focused on developing regulated diagnostics products. The ideal candidate will bring deep expertise in NGS technologies with a strong understanding of regulatory environments including CAP/CLIA and IVD product development. The successful candidate will play a crucial role in designing, developing, and optimizing our next generation of genomic assays. This position requires a unique blend of expertise in bioinformatics, extensive experience in assay optimization, analytical validation, strong skills in analytical pipeline development, automation and optimization, a deep understanding of molecular biology, and a passion for transforming complex biological data into actionable insights.KEY RESPONSIBILITIES:<ul><li>Lead bioinformatics design, development and validation efforts in assay development for new and on-market products. As part of project core teams, this individual must be responsible for coordinating planning, execution, and delivery within timelines and budget constraints.</li><li>Apply leading edge knowledge in bioinformatics, genomics, and assay technologies, to contribute to development of company's concepts and principles and to achieve assay development objectives in creative and effective ways.</li><li>Drive development study design and all analysis for assay development effort in collaboration with cross-functional teams.</li><li>Develop statistical and machine learning techniques to comprehensively evaluate assay performance and create optimization strategies.</li><li>Communicate analysis results, methodologies, and scientific findings to internal teams, external collaborators, and stakeholders.</li><li>Develop scalable, production-grade workflows for high-throughput NGS data analysis using AWS and containerized environments.</li><li>Facilitate successful production pipeline deployment by working closely with infrastructure and engineering teams</li><li>Ensure compliance with regulatory standards (CAP/CLIA, FDA, IVDR) throughout the bioinformatics development lifecycle, including rigorous testing and documentation.</li><li>Contribute to regulatory submissions and audits by providing technical documentation and validation reports.</li><li>Provide scientific guidance and mentorship to junior bioinformatics team members.</li></ul><h3>Who You Are:</h3>REQUIRED EXPERIENCE:<ul><li>PhD or MS in bioinformatics, computational biology, or an adjacent data science field, such as biostatistics, statistics or computer science.</li><li>Proven experience - A minimum of 6 -7 years of experience in bioinformatics analysis, algorithm development, and pipeline implementation.</li><li>Thorough understanding of NGS technologies and various methods for library preparation (WGS, enrichment, RNA-Seq, methylation, etc.).</li><li>Proficiency in quantitative transcriptomics from NGS or expression microarray data in human disease/biology specifically, such as differential expression, dimension reduction, expression-based classifier development, RNA-based signatures, cell type deconvolution.</li><li>Proficiency in machine learning, development of novel bioinformatics methodologies, and algorithms development, including benchmarking of computational methods.</li><li>Proven experience developing and deploying bioinformatics workflows in AWS (e.g., EC2, S3, Step Functions, Batch, Lambda, etc.).</li><li>Strong proficiency in Python, including experience with testing frameworks and SDLC best practices.</li><li>Close collaboration with Quality and Regulatory Affairs team on assay and analysis pipeline development and verification.</li><li>Demonstrated record of technical and scientific leadership, ownership, and independent work.</li></ul>RELEVANT EXPERIENCE (preferred but not required):<ul><li>Track record of working with wet lab scientists on iterative experiment design, execution, analysis, and interpretation as a tightly integrated team.</li><li>Proficiency in genomics, sequence analysis, and secondary analysis, such as variant calling (e.g., SNVs/MNVs/indels, CNV, structural variants), NGS QC, splicing, circular nucleic acids.</li><li>Strong understanding of germline and somatic mutation processes leading to complex variation and genome-wide biomarkers with potential clinical utility, such as TMB, mutational signatures, LOH.</li><li>Working knowledge of R.</li><li>Experience with relational and non-relational database technologies is a plus.</li><li>Excellent communicator about complex technical topics in an interdisciplinary setting, especially by using data visualizations and diagrams.</li><li>Excellent technical problem solving and troubleshooting skills.</li></ul>CULTURAL FIT:<ul><li>Passion for Innovation: You are deeply curious and driven to explore uncharted territories in genomics. Your passion for discovery motivates you to use novel analytical approaches to bring new insights to assay optimization and evaluation.</li><li> Collaborative Spirit: You thrive in a collaborative environment, bringing a positive, can-do attitude to interdisciplinary projects. You are skilled at communicating complex ideas to non-experts and active listening, fostering an inclusive atmosphere that values each team member's contribution. You are receptive to feedback and motivated to better serve the team’s needs.</li><li>Adaptability: In our fast-paced industry, change is constant. You are agile and flexible, ready to pivot strategies in response to new data or technologies. Your resilience and open-mindedness help our team navigate the uncertainties inherent in groundbreaking research.</li></ul>#LI-Hybrid, or #LI-RemoteFor candidates based in our San Diego office, the salary range is $160,000 - $180,000.For candidates based in our South San Francisco office, the salary range is $175,000 - $189,000. For candidates working remote (US), the salary range is $150,000 - $168,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units.Pay range$150,000—$189,000 USD<h3>What We Can Offer You</h3>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. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.<h3>About Veracyte</h3>Veracyte (Nasdaq: VCYT) 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, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.veracyte.com%2F&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=www.veracyte.com&amp;index=5&amp;md5=4d48386b00ece1531372e2e593d7cd2d" rel="noopener noreferrer">www.veracyte.com</a> or follow us on <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fveracyte%2F&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=LinkedIn&amp;index=6&amp;md5=234cba826cb637f449d2722139f551ef" rel="noopener noreferrer">LinkedIn</a> or <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fx.com%2Fveracyte%3Fs%3D11&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=X+%28Twitter%29&amp;index=7&amp;md5=20ead95735af622bf261b20735515b66" rel="noopener noreferrer">X (Twitter)</a>.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. View our <a href="https://www.veracyte.com/legal/privacy-statement-for-california-residents/" rel="noopener noreferrer">CCPA Disclosure Notice</a>If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to <a rel="noopener noreferrer">careers@veracyte.com</a>
Departments: 330 Bioinformatics &amp; Data Science

Sr. Bioinformatics Scientist

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. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions. Our Values:<ul><li>We Seek A Better Way: We pursue bold ideas, embrace complexity, and keep pushing forward.</li><li>We Make It Happen: We act with urgency, deliver with excellence, and always find a way. </li><li>We Are Stronger Together: We engage with empathy, align around what's best for Veracyte, and celebrate as one team. </li><li>We Care Deeply: We show up with integrity, kindness, and respect for one another. </li></ul><h3>The Position:</h3>Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Lead Specimen Processors are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility with work schedules including daily assignments, holiday schedules, and days of the week as determined by business need.The person in this position must be able to coordinate the integral daily tasks which consists of making sure that Specimen Processor personnel are performing their duties, maintaining flexibility with regards to work schedule including section assignment, daily work shifts, and days of the week as determined by business need to meet the quality needed for excellent patient care.ESSENTIAL DUTIES AND RESPONSIBILITIES include the same tasks as Senior SP in addition to the following. Other duties may be assigned.<ul><li>Proactively contributes to reaching team goals of cost-effective, high quality patient care services through leadership, technical expertise, and the appropriate utilization of resources.</li><li>Assists in the creation of, training, and implementation of departmental standard operation procedures.</li><li>Enhances existing procedures and services with quality that exceeds expectation.</li><li>Demonstrates the ability to take initiative, drive productivity, and build a collaborative environment. </li><li>Understands and performs laboratory activities to all applicable regulatory and compliance requirements.</li><li>Performs all duties according to guidelines outlined within the quality systems.</li><li>Participates in long term laboratory operations planning, including staffing, equipment, training schedules, and new assay implementation.</li><li>Demonstrates mastery in all related laboratory's established standard operating procedures and policies, involving specimen handling and processing, documentation/requisition, recording of processes in accordance with the Quality Assurance Program, and troubleshooting procedures for non-routine operations.</li><li>Develop and monitor on-going performance of employees, provide corrective action and counseling as required.</li><li>Responsible for training, coaching, supervision, on-boarding of new hires and development of staff.</li><li>Covers Supervisor duties in Supervisor absence including creating schedules and attending/participating in staff/quality meetings, and completing metrics.</li></ul><h3>Who You Are:</h3>Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Lead Specimen Processors are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility with work schedules including daily assignments, holiday schedules, and days of the week as determined by business need.The person in this position must be able to coordinate the integral daily tasks which consists of making sure that Specimen Processor personnel are performing their duties, maintaining flexibility with regards to work schedule including section assignment, daily work shifts, and days of the week as determined by business need to meet the quality needed for excellent patient care.ESSENTIAL DUTIES AND RESPONSIBILITIES include the same tasks as Senior SP in addition to the following. Other duties may be assigned.<ul><li>Proactively contributes to reaching team goals of cost-effective, high quality patient care services through leadership, technical expertise, and the appropriate utilization of resources.</li><li>Assists in the creation of, training, and implementation of departmental standard operation procedures.</li><li>Enhances existing procedures and services with quality that exceeds expectation.</li><li>Demonstrates the ability to take initiative, drive productivity, and build a collaborative environment. </li><li>Understands and performs laboratory activities to all applicable regulatory and compliance requirements.</li><li>Performs all duties according to guidelines outlined within the quality systems.</li><li>Participates in long term laboratory operations planning, including staffing, equipment, training schedules, and new assay implementation.</li><li>Demonstrates mastery in all related laboratory's established standard operating procedures and policies, involving specimen handling and processing, documentation/requisition, recording of processes in accordance with the Quality Assurance Program, and troubleshooting procedures for non-routine operations.</li><li>Develop and monitor on-going performance of employees, provide corrective action and counseling as required.</li><li>Responsible for training, coaching, supervision, on-boarding of new hires and development of staff.</li><li>Covers Supervisor duties in Supervisor absence including creating schedules and attending/participating in staff/quality meetings, and completing metrics.</li></ul>REQUIREMENTS: QUALIFICATIONSTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.EDUCATION and/or EXPERIENCE<ul><li>4-5 years of accessioning experience and/or in a lab setting</li><li>High school diploma or equivalent required</li><li>Bachelor’s degree preferred.</li><li>Excellent verbal and written communication skills</li><li>The ability to navigate efficiently through, or have familiarity with, various Laboratory Information Systems (LIS) and have proficiency in Microsoft Office products (Excel, Word, Access and PowerPoint).</li><li>Excellent judgment and problem-solving skills</li><li>Excellent teamwork and collaborations skills</li><li>Ability to work independently</li><li>Enthusiasm and an entrepreneurial spirit</li></ul>PHYSICAL REQUIREMENTS<ul><li>Repetitive movement of hands, arms and legs</li><li>Repetitive movement of fingers (typing and/or writing)</li><li>Sitting, with occasional walking, standing, stooping and moving about</li><li>Talking and hearing</li><li>Occasionally required to lift up to 25 pounds</li></ul>#LI-OnsiteFor candidates based in our San Diego office, the hourly range is $29.00-$33.00.The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units.Pay range$29—$33 USD<h3>What We Can Offer You</h3>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. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.<h3>About Veracyte</h3>Veracyte (Nasdaq: VCYT) 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, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.veracyte.com%2F&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=www.veracyte.com&amp;index=5&amp;md5=4d48386b00ece1531372e2e593d7cd2d" rel="noopener noreferrer">www.veracyte.com</a> or follow us on <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fveracyte%2F&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=LinkedIn&amp;index=6&amp;md5=234cba826cb637f449d2722139f551ef" rel="noopener noreferrer">LinkedIn</a> or <a href="https://cts.businesswire.com/ct/CT?id=smartlink&amp;url=https%3A%2F%2Fx.com%2Fveracyte%3Fs%3D11&amp;esheet=54340020&amp;newsitemid=20251015446872&amp;lan=en-US&amp;anchor=X+%28Twitter%29&amp;index=7&amp;md5=20ead95735af622bf261b20735515b66" rel="noopener noreferrer">X (Twitter)</a>.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. View our <a href="https://www.veracyte.com/legal/privacy-statement-for-california-residents/" rel="noopener noreferrer">CCPA Disclosure Notice</a>If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to <a rel="noopener noreferrer">careers@veracyte.com</a>
Departments: 203 Accessioning

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