Scientist, IVD Product Development & Validation

Predicine; Hayward (CA); On-site; USD 100,000 - 140,000; Full time

Job summary

Predicine is seeking a Scientist for IVD product development and validation in Hayward, CA. The role focuses on designing, executing, and analyzing analytical validation studies for Predicine's NGS-based IVD products, with close collaboration across Laboratory Operations, Quality, Regulatory, and Bioinformatics.

The ideal candidate has strong molecular biology/NGS experience, excellent attention to detail, and a drive to advance regulated diagnostics from lab to clinic.

Qualifications

• Experience designing and executing validation studies for NGS-based assays.
• Strong scientific writing for protocols, reports and regulatory documents.
• Ability to interpret complex data and troubleshoot validation results.

Responsibilities

• 30% Validation study design and execution per regulatory requirements.
• 20% Coordination of sample prep, testing, and data generation.
• 20% Prepare validation protocols and technical summaries.
• 20% Support regulatory submissions and data readiness.
• 10% Present results to cross-functional teams and stakeholders.

Skills

Experimental Design

Data Analysis

Troubleshooting

Lab Procedures

NGS Knowledge

Regulatory Awareness

Communication Skills

Urgency & Motivation

Education

PhD in Molecular Biology

Bachelor’s/Master with 3+ years experience

Tools

NGS Platforms

Job description

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Scientist, IVD Product Development & Validation

Full Time Professional Hayward, CA, US

About Predicine Inc.

Predicine Inc. is a Silicon Valley-based global precision diagnostic company committed to developing first- and best-in-class liquid biopsy cancer diagnostics assays. We provide innovative blood- and urine-based molecular diagnostic tests to enable precision medicine. Predicine's liquid biopsy platform and molecular insight solutions help biopharma companies accelerate drug development and expand discovery in oncology. We partner with the top 10 leading global biopharma companies to support biomarker-driven clinical trials across the US, EU, and APAC, including China. At Predicine, we believe people are our most important asset, and we're dedicated to creating a great place to work — one built on creativity, integrity, accountability, productivity, and teamwork.

Job Summary

We are seeking a highly motivated Scientist to support the development, analytical validation, and regulatory submission of Predicine's NGS-based IVD products. This position will play a key role in designing and executing analytical validation studies, analyzing and interpreting validation data, preparing technical documentation, and supporting regulatory submissions. The scientist will work closely with cross-functional teams — including Laboratory Operations, Quality, Regulatory, and Bioinformatics — to ensure validation studies are scientifically sound, executed according to approved protocols, and completed within established timelines. The ideal candidate brings strong experience in molecular biology and/or NGS, excellent experimental and analytical skills, strong attention to detail, and genuine interest in applying scientific knowledge to regulated IVD product development.

What You'll Do

Key Responsibilities & Time Allocation

30%- Validation Study Design & Execution — Design and execute validation studies for NGS-based IVD assays in accordance with design control and applicable regulatory requirements; develop and review study protocols, experimental plans, and acceptance criteria based on intended use, product requirements, risk assessment, and regulatory expectations.

20%- Study Coordination & Data Generation — Coordinate sample preparation, laboratory testing, and data generation to ensure studies are executed according to approved protocols and timelines; support investigation and resolution of unexpected results, study deviations, and other validation-related issues.

20%- Technical Documentation — Prepare and maintain validation protocols, reports, technical summaries, and other product development documentation; ensure technical documents are scientifically accurate, complete, traceable, and consistent with applicable regulatory and quality requirements.

20%- Regulatory Submission Support — Support preparation of technical documentation required for regulatory submissions and reimbursement assessments; organize and maintain validation data and supporting documentation to ensure readiness for regulatory review.

10%- Cross-Functional Collaboration & Presentation — Present validation results and technical conclusions to cross-functional teams and stakeholders; work closely with Regulatory and Quality teams to ensure submission materials are complete, consistent, and aligned with applicable requirements.

Required Skills & Qualifications

• Strong skills in experimental design, data organization, and result interpretation
• Familiarity with laboratory procedures, SOPs, and instruments
• Critical thinking and effective troubleshooting skills
• Solid knowledge of NGS-related research areas such as NGS, molecular biology, genetics, cancer biology, or related areas
• Willingness to work in the lab and learn FDA and other regulatory authorities' guidelines on general principles related to validations
• Proficient reading and communication skills
• Highly self-motivated with a strong sense of urgency

Education

PhD in Molecular Biology or a closely related field or Bachelor's/Master's degree with 3+ years of applicable technical experience

Field of Study

Experience Preferred

• PhD holders: no additional minimum experience specified
• Non-PhD candidates: 3+ years of technical experience in applicable areas such as NGS or oncology

Join Us

At Predicine, you won't just run experiments — you'll help bring regulated, first-of-their-kind cancer diagnostics from the lab to real-world clinical use. If you're detail-driven, scientifically rigorous, and want to make a direct impact on how cancer is diagnosed, we want to hear from you.

Predicine is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.