Roche

Principal Bioinformatics Scientist I

Roche$115K — $151K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master’s degree with 7+ years relevant experience or Ph.D. with 4+ years in a related field.
  • Experience in a CAP/CLIA-certified laboratory for diagnostic test development.
  • Proficiency in high-throughput sequencing data analysis.
  • Strong programming skills in Python, R, or C++ and familiarity with cloud and container technologies.
  • Proven experience in cross-disciplinary collaboration and stakeholder management.

Responsibilities

  • Design and optimize scalable, reproducible NGS bioinformatics pipelines.
  • Partner with assay development teams to validate diagnostic methodologies.
  • Integrate AI tools into data analysis workflows and algorithm development.
  • Draft technical specifications for clinical software development.
  • Implement statistical quality control metrics aligned with regulatory standards.
  • Enforce standard software engineering practices across projects.

Benefits

  • Collaborative environment with cross-functional teams for innovation.
  • Engagement in next-generation diagnostic technology development.
  • Opportunity to work in a CAP/CLIA-certified environment.
  • Strong focus on precision medicine and patient outcomes.
Full Job Description
The Position

Principal Bioinformatics Scientist I

This role is a vital part of our Bioinformatics team, which is committed to advancing precision medicine by building cutting-edge computational tools for clinical diagnostics. As a member of this team, you will sit at the dynamic intersection of computational biology, assay development, and software engineering to translate complex genomic data into actionable health insights.

You will have the opportunity to collaborate closely with cross-functional partners across Wet-Lab Assay Development, Software Engineering, CLIA Operations, and Quality to design, validate, and operationalize next-generation diagnostic tests.

The Opportunity

As a Bioinformatics Scientist, you will lead the design, optimization, and clinical validation of innovative NGS data processing pipelines and algorithms. You will serve as the technical bridge between wet-lab innovation and production-grade software engineering, leveraging advanced statistical modeling and modern AI coding tools to deliver high-accuracy molecular diagnostics for patient care.

  • Pipeline & Algorithm Development: Design, benchmark, and optimize scalable, reproducible NGS bioinformatics pipelines using Nextflow, Docker/Singularity, and cloud environments.

  • Analytical Validation:Partner with Assay Development and CLIA lab teams to establish statistical analysis plans and validate novel diagnostic assays (ensuring high sensitivity, specificity, and precision).

  • AI-Accelerated Engineering: Routinely integrate AI coding tools and automated workflows to accelerate algorithm development, refactoring, and data analysis.

  • Production Translation: Draft clear functional and technical specifications to guide software engineering teams in transitioning research prototypes into robust clinical software.

  • Quality & Regulatory Compliance: Implement sample- and run-level statistical QC metrics while maintaining thorough QMS-compliant documentation for CAP/CLIA audits.

  • Best Practices:Enforce high-standard software engineering practices, including Git version control, continuous integration, unit testing, and modular architecture.

Who You Are

  • Education & Experience: Master’s degree with 7+ years of related experience; OR Ph.D. with 4+ years of related experience (work experience can be prior or post-grad; relevant post-grad academic lab training will be considered).

  • Matrixed Collaboration & Stakeholder Management: Proven ability to partner seamlessly across multidisciplinary teams—including wet-lab scientists, software engineers, lab directors, and Quality assurance—to align technical specs with clinical goals.

  • Clinical Diagnostic Expertise:Demonstrated track record supporting or working within a CAP/CLIA-certified laboratory environment with direct experience in diagnostic test development and analytical validation.

Technical Mastery

  • Deep understanding of high-throughput sequencing data analysis across various modalities (targeted panels, WGS/WES, transcriptomics, or liquid biopsy/ctDNA).

  • Proficient in Python/R/C++ and Linux/Bash alongside hands-on experience using workflow managers (Nextflow) and containerized software deployments.

  • Modern Workflow Adaptability:Proven ability to leverage AI development tools to maximize productivity, alongside excellent communication skills suited for navigating complex, cross-functional organizational environments.

Relocation benefits are not available for this position.

The expected salary range for this position based on the primary location of Mississauga is 115,328.00 and 151,368.00 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

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