Senior Development Scientist I

Why join Freenome?

Freenome is a high-growth biotech company developing tests to detect cancer using a standard blood draw. To do this, Freenome uses a multiomics platform that combines tumor and non-tumor signals with machine learning to find cancer in its earliest, most-treatable stages. 

Cancer is relentless. This is why Freenome is building the clinical, economic, and operational evidence to drive cancer screening and save lives. Our first screening test is for colorectal cancer (CRC) and advanced adenomas, and it’s just the beginning. 

Founded in 2014, Freenome has ~400 employees and continues to grow to match the scope of our ambitions to provide access to better screening and earlier cancer detection.  

At Freenome, we aim to impact patients by empowering everyone to prevent, detect, and treat their disease. This, together with our high-performing culture of respect and cross-collaboration, is what motivates us to make every day count.

Become a Freenomer

Do you have what it takes to be a Freenomer? A “Freenomer” is a determined, mission-driven, results-oriented employee fueled by the opportunity to change the landscape of cancer and make a positive impact on patients’ lives. Freenomers bring their diverse experience, expertise, and personal perspective to solve problems and push to achieve what’s possible, one breakthrough at a time.

About this opportunity:

At Freenome, we are seeking a Senior Development Scientist I to help grow the Freenome Genomic Early Development team. The ideal candidate will serve as a subject matter expert and technical lead in the development and optimization of new and existing NGS assay workflows and processes. You will collaborate extensively with the Molecular Research, Computational Science, Late Development, Manufacturing, Quality, Regulatory & Program Management teams to develop and transfer technologies into a regulated, high-throughput environment and contribute to Freenome’s multiomic product portfolio aimed at early cancer detection. You will use your analytical and programming abilities to identify ways to rapidly iterate and improve on existing methods, and you will work closely with computational biologists to evaluate technologies that can enhance our end-to-end test performance.

This role reports to the Senior Manager, Development. This role will be an onsite role based in our Brisbane, California headquarters. 

What you’ll do:

• Applies knowledge of molecular biology, nucleic-acid biochemistry, and next-generation sequencing to develop and optimize assays for DNA and other bioanalytes, including genome-wide and targeted approaches, by following principles of Design Controls for IVD product development
• Provides hands-on technical expertise in the prototype assay tech transfer from Research to Development, and leads subsequent Design and Development of NGS assays into high throughput automated assays with improved performance in early cancer detection
• Develops and characterizes new reagents, controls, automated processes, and define in process controls and assay performance requirements
• Develops R&D tools to troubleshoot root cause of workflow failure and proposes solutions to improve assay performance and robustness
• Leads from the bench by training and mentoring junior team members while also performing your own experiments in order to facilitate rapid progress toward project goals
• Participate in project planning and prioritization through a deep understanding of company objectives and available resources, and reprioritizes as needed, and collaborate with appropriate stakeholders to more effectively plan
• Collaborates with Quality Control Lab, Manufacturing lab, Quality, and Regulatory to transfer reagent quality control methods and manufacturing processes from Development to Operations
• Maintains detailed records of experiments, data, results and methodologies in compliance with Good Laboratory and Documentation Practices (cGLP, cGDP), authors study protocols and reports, contribute to work instructions and record forms in collaboration with Operations

Must haves:

• A Ph.D with at least 6 years of related experience or a Bachelor’s degree with at least 12 years of related experience in molecular biology, biochemistry, genetics, or a related field with experience in NGS-based assay development
• In-depth technical knowledge and extensive hands-on experience in NGS based assay development including sample preparation, nucleic acid extraction, library preparation, target capture, a