Staff Scientist, IVD Product Development

POSITION SUMMARY:

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.

We are looking for a highly motivated Staff Scientist with a strong focus on reagent and process optimization to join the Early Cancer Detection product development team, joining a group of scientists who are tasked with developing and advancing Natera’s oncology product portfolio.

The Staff Scientist will be working with internal cross functional teams to develop IVD products. 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 Scientist should have an in-depth understanding of design control methods and experience with current NGS oncology diagnostics devices.

We are looking for a meticulous and proactive scientist with experience in NGS-based assay development under design control and meant for submission to FDA and other regulatory bodies and who can work effectively in a fast-paced environment to ensure that the highest quality clinical assays are developed and launched for our patients.

PRIMARY RESPONSIBILITIES:

• Design, develop and validate automated high-throughput NGS assays that will be run in a commercial CLIA laboratory
• 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, Excel)
• Collaborate with other assay development scientists on the specifications of assay, reagent, equipment and quality metrics for future production assays
• Work with Clinical Laboratory and Quality Assurance to ensure that developed methods meet Natera’s rigorous quality standards
• Coordinate with multiple internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) and serve as point person to ensure the successful and timely execution of projects
• Write study protocols and reports and SOPs and train lab operations operators on protocols
• Lead verification activities
• 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
• Ability to manage Scientists and Research Associates

QUALIFICATIONS:

• MS with 11+ years or PhD with 8+ years experience in assay development and automation for the life science industry.
• Demonstrated track record of development and validation of automated protocols for CLIA labs
• Experience with IVD product development and design controls
• Deep technical knowledge of NG