About the Company:
Natera is a San Carlos, CA-based company that is driven by a passion for elevating the science and utility of prenatal testing. The advent of the Information Age has created a paradigm shift in the fields of computing and informatics. Surprisingly, medical diagnostics have been slow to integrate these advances into genetic testing. Until Natera.
From conception to delivery, Natera is pioneering next-generation accuracy and reliability in preconception and prenatal genetic testing services, enabling couples to be informed about their pregnancy each step of the way. The company offers a wide range of tests from preimplantation genetic diagnosis (PGD) for IVF to breakthrough advances in the field of non-invasive prenatal testing (NIPT). Using advances from the human genome project and powered by sophisticated proprietary bioinformatic algorithms, Natera’s comprehensive portfolio of tests, proven science, and experienced genetic counseling services deliver the most accurate results in the industry.
Job Title: Senior Scientist
Natera is currently seeking a Senior Scientist within the Process Development Group would lead the conversion of new analytical test methods into robust commercial products to support the processing of patient samples in a regulated clinical molecular and genetic diagnostics laboratory environment. The incumbent will collaborate with internal and external research scientists, statisticians and engineers to test, validate, implement and be the technical and scientific point person for the newly developed diagnostics tests.
Responsibilities:
- Leadership, project planning, Assay development, technology transfer, product launch, process improvements and product support
- Assay Optimization and Development of Analytical Methods to support NGS and Sanger Sequencing
- Be data driven with strong data analysis skills
- Development and validation of methods for high throughput adaptation
- Interface with CRO and also work closely with Research, Automation Engineers, Bioinformatics, Statistics and other cross-functional teams within the company
- Track progress of project, be flexible, be able to handle multiple projects and help drive key decisions with solid testing data and scientific leadership
- Strong and effective communication skills, including writing protocols, testing plans, development and validation reports
- Strong troubleshooting skills
- Manage timelines, estimate risk and set priorities
- 10% Travel may be needed at various product development stages
Qualifications:
- Ph.D in molecular biology, Genetics or related fields with a minimum of six years of experience leading the development, optimization, and implementation of molecular and genetic diagnostic tests in CLIA or FDA regulated laboratory environment
- Hands-on scientist with substantial experience with laboratory method and workflow optimization of molecular biology assays for high-throughput laboratory operations
- Data driven with strong skills using JMP, Excel and other data analysis tools
- Skilled at writing clear SOPs and Validation reports, and experience with quality management, including design control, risk analysis and mitigation strategies
- Deep understanding of essential molecular biology and methods such as PCR, DNA purification, analysis tools DNA quantitation, and quality control is required
Preferred Skills:
- Next generation sequencing and development and support of reagents, tests, documentation, workflows or automation for CLIA laboratories a plus
- Project management skills would be a plus
- Previous experience in development/validation of CLIA or FDA regulated assays would be a plus
How to Apply:
Eligible candidates click the link below to apply.
Apply Online
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