Bioinformatics Scientist II

Sorry, this job was removed at 06:09 p.m. (CST) on Friday, Apr 04, 2025
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2 Locations
In-Office
116K-155K Annually
Healthtech • Information Technology • Biotech
The Role

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 – whether it be in one of our labs, corporate offices, the field – enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a results-driven environment that values innovation, collaboration, and compassion.

The Position:

We are seeking an exceptionally talented Bioinformatics Scientist to join our group in our Data Analysis Team (DAT).  This individual will be responsible for constructing, updating, and monitoring robust quality control (QC) processes for microarray and NGS-based high-volume Laboratory Developed Test (LDT) disease diagnostic products run in CLIA labs, with a primary focus on RNA-based assays. The role involves overseeing the day-to-day work maintaining operational excellence of our products, providing guidance for process improvements, and troubleshooting efforts in collaboration with cross-functional teams.

The successful candidate will play a vital role in ensuring the execution of life-saving diagnostic products and ensure consistent performance throughout routine CLIA updates, including reagents, equipment, and processes. This role will also actively support design verification and validation test plans, protocols, procedures, and reports and actively participate in cross-functional design reviews.

Working in a well-supported environment, the candidate will have access to the tools, technologies, and expertise necessary for success. In this intensely collaborative and fast-paced environment, the individual will gain valuable knowledge in diagnostic product development and sustaining, while experiencing the swift implementation of their efforts towards products that will transform patient lives.

This is a hybrid position based in our San Diego or South San Francisco, CA office. Candidate will be required to work Pacific Time hours.

Essential Requirements Include:

  • A Master’s or Ph.D. in Bioinformatics, Computational Biology, or related field of study.
  • Minimum of 2 years (Ph.D.) or 4 years (M.Sc.) of relevant work experience, with demonstrated expertise in working with high-throughput.
  • Working knowledge of genomics and molecular biology.
  • Strong analytical skills and demonstrated proficiency in programming languages such as R, and/or Python.
  • Experience in data visualization, data wrangling, and SQL is required.
  • The candidate should have hands-on experience with high-dimensional data and cutting-edge bioinformatics pipelines.
  • Comfort with Linux-based operating systems and good software engineering practices including maintaining code via version controlled systems (e.g., GitHub, Bitbucket).
  • Experience with AWS Services, S3, EC2.
  • Experience in building R shiny apps or data dashboards with BI tools such as Tableau.
  • Excellent written and verbal communication and presentation skills are required.
  • Ability to translate complex computational concepts in such a way that scientifically trained individuals in other disciplines can readily understand their significance.

Who You Are:

  • Passionate about genomics and data science.
  • Deeply committed to improve patient lives.
  • Motivated to use novel analytical approaches to bring new insights to biological problems.
  • The ability to research solutions to new problems; rapidly learn and adopt new methods as necessary.
  • Enthusiastic, collaborative, and positive "can-do" attitude is a must.
  • Thrives in an environment of shared goals and responsibilities.
  • A great team player with solid technical training and always apply the highest scientific rigor.
  • Ability to be highly productive under aggressive and tight timelines; fast adapter to change with a calm and steady energy.
  • Skilled in active listening, welcomes feedback from others, and constantly strives for improvement to better serve the team’s needs.

Preferred Skills:

  • Prior experience working with clinical tests in a regulated environment (i.e., CAP, CLIA, NYS, ISO 15189, ISO13485).
  • Working experience in regulated diagnostic assay development.


#LI-Hybrid


The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the 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. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.

Pay range

$116,000$155,000 USD


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. 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.


About Veracyte

Veracyte (Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. Veracyte is based in South San Francisco, California. For more information, please visit www.veracyte.com and follow the company on X (Formerly Twitter).

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 CCPA Disclosure Notice.

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 [email protected]

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The Company
Austin, TX
596 Employees
Year Founded: 2008

What We Do

Veracyte is a global diagnostics company that empowers 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 growing menu of diagnostic tests answers important clinical questions to help patients avoid risky, costly procedures and interventions, and accelerate time to appropriate treatment

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