Illumina Inc

Staff Scientist

Illumina Inc$118K — $177K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years in IVD assay development or related fields (Bachelor's); 6+ years with Master's; or 3+ years with PhD.
  • Strong background in next-generation sequencing and molecular diagnostics.
  • Experience with regulatory submissions and compliance (CLSI and ISO 13485).
  • Proven ability in experimental design, data analysis, and troubleshooting.
  • Demonstrated leadership and mentorship capabilities in a scientific setting.

Responsibilities

  • Provide technical leadership in IVD oncology assay and kit development.
  • Guide assay product development by applying knowledge of IVD requirements and clinical workflows.
  • Drive technical improvements in functional and project teams execution.
  • Lead verification and validation protocols development and documentation.
  • Maintain research documentation in accordance with Quality Management Systems.
  • Supervise and develop team members in scientific study execution.
  • Authorship of project reports and presentations to senior leadership.

Benefits

  • Access to genomics sequencing services.
  • Comprehensive family planning support.
  • Health, dental, and vision insurance.
  • Retirement benefits.
  • Generous paid time off policy.
Full Job Description
Illumina is seeking a Staff Scientist with expertise in IVD assay development and next-generation sequencing to advance molecular diagnostics and precision oncology. This role is part of the Clinical Solutions team supporting pharma-collaborative projects through assay development, formal verification and validation testing, clinical studies, and regulatory submission. The Staff Scientist serves as a Study Lead and technical subject matter expert for assigned studies and technical workstreams, with responsibility for experimental design, data analysis and verification, protocol and report authorship, troubleshooting, and cross-functional decision-making within those areas. The role collaborates closely with internal partners, including Quality, Regulatory, Clinical Affairs, Biostatistics, Software, Bioinformatics, and Operations, as well as external partners, to contribute to project goals and deliverables, present results, identify risks and mitigations, and recommend solutions. At the Staff Scientist level, the position includes expanded technical leadership, mentorship, and business acumen responsibilities. Key Responsibilities: 3 Provide technical leadership for the initiation, planning, development, troubleshooting, and validation of IVD oncology assays and kits for the clinical market3 Apply knowledge of IVD product requirements, clinical laboratory workflows, and clinical market needs to guide assay and product development decisions3 Drive technical decision-making and continuous improvement across functional and project teams responsible for designing, executing, troubleshooting, analyzing, and presenting experiments3 Lead team execution of formal IVD verification and validation protocols and regulatory reports based on CLSI and other applicable industry standards3 Document research progress and study outcomes within a Quality Management System consistent with ISO 13485 expectations3 Manage and develop scientists through the design, execution, troubleshooting, analysis, and documentation of verification and validation studies3 Author reports and present results, project updates, risks, mitigations, technology assessments, and technical roadmaps to colleagues, senior management, and leadership Experience/Education: 3 Typically requires a minimum of 8 years of related experience with a Bachelor's degree; or 6 years and a Master's degree; or a PhD with 3 years of experience; or equivalent experience. The estimated base salary range for the Staff Scientist role based in the United States of America is: $118,200 - $177,200. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. The range reflects long-term growth in the role; therefore, most candidates are hired between the minimum and middle of the range. Placement depends on experience, skills, location, and internal equity. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.

About Illumina Inc

Illumina, Inc. is an American company incorporated in April 1998 that develops, manufactures and markets integrated systems for the analysis of genetic variation and biological function. The company provides a line of products and services that serves the sequencing, genotyping and gene expression markets. Its headquarters are located in San Diego, California.
Learn more about Illumina Inc
Size
9,800 employees
Market Cap
$30.3 billion
Industry
Net Income
$656 million
Founded
1998
5 Year Trend
+13.5%
Revenue
$3.2 billion
NASDAQ

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