Staff Scientist, New Product Development

San Carlos, United StatesHybrid

Responsibilities

Design, develop, and validate automated high-throughput NGS assays that will be run in a commercial CLIA laboratory
Provide production support to automated high-throughput NGS assays currently run in commercial CLIA laboratories
Manage assigned technical projects and associated timelines and deliverables in NGS-based assays. Mentor and manage the functional activities of junior employees
Design and execute moderate to high complexity experiments and perform data analysis (e.g. JMP, R, Python, Excel)
Coordinate with multiple internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) and serve as point person/technical lead to ensure the successful and timely execution of projects
Write study protocols, reports, and SOPs, train lab operations operators on protocols
Identify areas for continuous improvement and actively contribute to the effort of introducing better practices to improve production workflows and shorten TAT for patient samples
Demonstrated track record of development and validation of automated protocols for CLIA labs

experience in next generation sequencing (NGS) assay development who enjoys solving challenging and complex problems in a fast-paced environment.
The ideal candidate is a driven professional who maintains broad knowledge of molecular biology and chemistry, and applies statistical principles to experiment design and analysis.
The candidate should have an in-depth understanding of product development and support in a CLIA environment, and
experience with current NGS oncology diagnostics devices. PRIMARY RESPONSIBILITIES:
Ability to manage Scientists and Research Associates
experience in assay development and automation for the life science industry.
Well able to perform first-pass data analysis; strong ability to interpret experimental data
Deep technical knowledge of NGS biology and processes
Strong understanding of the chemistry underlying nucleic acid extraction, PCR, NGS library preparation, and hybrid capture technologies •
Experience designing and executing studies including stability, guard banding, reproducibility and repeatability and QC method development
Data analysis (JMP, Python, or R) required
Ability to manage multiple priorities in a fast-paced, dynamic environment and to collaborate cross-functionally with other groups (regulatory, CLIA, LIMS, automation, research, product)
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.

Natera is a global leader in cell-free DNA testing. We measure fetal, tumor, or donor cfDNA at the molecular level to help inform personalized health care decisions with a non-invasive test.
Compensation & Total Rewards
This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.
This position is also eligible for additional compensation and
benefits through Natera’s robust Total Rewards program, including: •
Annual performance incentive bonus •
Long-term equity awards •
Comprehensive health benefits (medical, dental, vision) •
Generous paid time off and company holidays •
Compensation Range $157,300 — $196,600 USD OUR OPPORTUNITY
Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other
benefits include pregnancy and baby bonding leave, 401k benefits, commuter

For more information, visit www.natera.com .
Link: https://www.natera.com/notice-of-data-collection-california-residents/
Please be advised that Natera will reach out to candidates with a @ natera.com email domain ONLY.

The ideal candidate is self-motivated and effectively works around unknowns to move the needle in the development, launch, and support of the highest quality clinical assays for our patients.
The Staff Scientist will be working with internal cross functional teams to develop, launch, and support LDT products.
Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera’s rigorous quality standards
Experience implementing, optimizing, and troubleshooting high-throughput automated assays utilizing liquid handler robots
Excellent communication, organization, record-keeping, planning, attention to detail and time management skills
Able to travel to Natera’s Austin site up to 20% of time
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
When you join Natera, you’ll work hard and grow quickly.
Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management. WHAT WE OFFER Competitive Benefits - Employee
benefits and much more. We also offer a generous employee referral program!