Scientist II, Assay Development
Foresite Labs Fl2024 006
| Company | Foresite Labs Fl2024 006 |
| Category | Science & Research |
| Location | San Diego |
| Remote | Hybrid |
| Employment | Not stated |
| Level | Not stated |
| Salary | USD 110k–120k |
| Posted | 17 Jul 2026 |
| Last verified | 12 Aug 2026 |
| Source | Employer ATS (ashby) |
Description
Scientist II, Assay Development
Location: San Diego, CA
Job Type: Full-Time
Salary $110,000 - $120,000
About Us
We are a venture-backed, stealth-stage biotechnology company based in San Diego, focused on developing novel technologies that will redefine how disease is detected, characterized, and managed with a novel approach to clinical genomics. Our mission is to fundamentally transform healthcare through a convergence of innovation across multiple scientific disciplines.
Founded by industry veterans with decades of experience in life sciences tools and diagnostics, our leadership team brings a proven track record of translating scientific insight into successful commercial products. Our investors include some of the most respected names in healthcare and deep tech.
Position Overview
We are seeking a Scientist II to support the development, optimization, and maturation of molecular methods for clinical next-generation sequencing (NGS) assays. This is a hands-on, bench-focused individual contributor role: executing the experiments that move nucleic acid extraction and library preparation methods from feasibility toward robust, automation-ready processes suitable for transfer to clinical lab operations.
Working closely with senior scientists and process engineers, the Scientist II will run structured experiments, generate and analyze high-quality data, and contribute to the optimization of buffer formulations, reaction conditions, and process parameters that drive method performance and stability. The role is well suited to a scientist with strong molecular biology fundamentals and solid bench execution who is ready to grow toward independent method development in a rigorous, quality-oriented environment where methods are actively evolving.
Key Responsibilities
- Execute bench experiments that advance library preparation methods from feasibility toward production-ready performance.
- Prepare and test buffer formulations and reaction conditions, and contribute to method optimization by generating and analyzing systematic, well-controlled data.
- Execute systematic experiments, and perform data analysis to characterize method performance.
- Run stability and robustness studies per established protocols, and summarize results clearly.
- Support the transfer of bench methods including hands-on protocol execution, method-comparison runs, and troubleshooting.
- Contribute to reagent QC by executing QC assays.
- Support tech transfer and analytical validation activities through bench execution, troubleshooting, and documentation.
- Maintain rigorous, well-organized experimental records (electronic lab notebook), generate clear data summaries and technical reports, and contribute to process and design documentation.
- Collaborate with assay development, process engineering, automation, quality, and clinical operations to advance methods from feasibility through production.
Qualifications
Required:
- BS in Molecular Biology, Biochemistry, Chemistry, or a related field with 3+ years of relevant laboratory experience; or MS with 2+ years; or a PhD in a relevant field.
- Solid molecular biology and biochemistry fundamentals, with hands-on experience in library preparation and workflows.
- Demonstrated bench proficiency in core techniques, with accurate, reproducible execution and strong attention to detail.
- Working familiarity with structured experimental design and data analysis.
- Rigorous, well-organized record-keeping and the ability to generate clear technical data summaries.
- Ability to execute independently on assigned experiments and manage parallel bench work in a fast-moving, early-stage environment.
Preferred:
- Experience with low-input or other challenging workflows.
- Hands-on experience with liquid handling platforms.
- Exposure to a regulated or quality-driven environment and familiarity with design controls.
- Programming or scripting experience (Python, R) for data ana