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Natera

Makes genetic tests for clinical care

Senior Design Transfer Scientist - R&D Design Transfer & Product Development

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSan Carlos, CA, USAIn-person

About the Job

Requirements

  • A PhD in Molecular Biology, Cell Biology, Biotechnology, Biochemistry, or a related scientific field with 4 or more years of relevant industry experience; or a Master's degree in those fields with 7 or more years of relevant industry experience; or a Bachelor's degree in those fields with 10 or more years of relevant industry experience.
  • Hands-on expertise in Next-Generation Sequencing workflows such as DNA/RNA extraction, targeted enrichment, or whole genome library preparation, and/or deep expertise with other DNA molecular biology techniques such as PCR, quantitative PCR, and multiplex PCR.
  • Ability to own a study from start to finish, including designing experiments, executing laboratory work, analyzing data, documenting results, and performing basic statistical analysis.
  • Knowledge of Design Controls, Quality Management Systems, and regulatory standards including FDA, ISO 13485, and CLSI within GLP/GMP environments is highly desired.
  • Experience authoring study plans, protocols, and study reports is highly desired.
  • Experience with statistical software such as JMP is highly desired.
  • Prior experience in in vitro diagnostic product development or commercialization is preferred.
  • Experience in manufacturing, scale-up, and Quality Control is preferred.
  • Experience with automated liquid handling platforms such as Hamilton or Tecan is preferred.

Responsibilities

  • Plan and execute process validations (IQ/OQ/PQ), stability studies, and study protocols; perform data analysis and author final reports.
  • Support test method development, characterization, and Test Method Validation, including the generation of manufacturing specifications.
  • Lead Risk Management activities, including Failure Mode and Effects Analyses, to identify and mitigate product risks; establish and maintain Design History Files and Device Master Records.
  • Lead change-control activities to evaluate and determine the impact of design changes to on-market products.
  • Investigate product or process deviations, perform root cause analysis, and implement Corrective and Preventive Actions.
  • Partner with Supply Chain to establish raw material and consumable pipelines; present status updates, data, and technical proposals to cross-functional stakeholders.

Desired Qualifications

  • Knowledge of Design Controls, Quality Management Systems, and regulatory standards including FDA, ISO 13485, and CLSI within GLP/GMP environments.
  • Experience authoring study plans, protocols, and study reports.
  • Experience with statistical software such as JMP.
  • Prior experience in in vitro diagnostic product development or commercialization.
  • Experience in manufacturing, scale-up, and Quality Control.
  • Experience with automated liquid handling platforms such as Hamilton or Tecan.

About the Company

Natera

Makes genetic tests for clinical care

Natera develops genetic tests for clinicians caring for people with cancer, inherited conditions, pregnancies, and organ transplants, using DNA analysis to inform medical decisions. Its portfolio includes Signatera for tracking residual cancer, Panorama for prenatal screening, and Prospera for assessing transplanted organ health. The company combines laboratory analysis with software that distinguishes DNA fragments in blood, and earns revenue mainly from diagnostic testing, alongside licensing and services for research partners. Clinicians use its portals to order tests, track samples, and review results, while patients have access to genetic information sessions. Natera was founded in 2004 and is headquartered in Austin, Texas.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Austin, TX
Founded
2004

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