Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. They are seeking a Software Test Engineer to design, develop, and execute test cases for laboratory systems while ensuring compliance in a regulated environment.
Responsibilities:
- Design, develop, and execute test cases based on software requirements, functional specifications, and user needs for laboratory systems
- Perform manual and/or automated testing to validate software functionality, data integrity, and workflow performance in a CLIA-regulated environment
- Partner closely with laboratory operations teams to understand end-to-end workflows and translate them into effective test scenarios
- Identify, document, and track software defects; collaborate with engineering teams to troubleshoot and resolve issues
- Support validation and verification activities for new software releases, system upgrades, and process changes in accordance with CLIA, CAP, NYSDOH, and internal quality standards
- Ensure traceability between requirements, test cases, and validation documentation
- Participate in risk assessments and impact analyses related to software changes affecting laboratory operations
- Contribute to the development and continuous improvement of software testing strategies, SOPs, and documentation practices
- Support audits and inspections by maintaining clear, thorough, and compliant testing documentation
- Act as a quality advocate, ensuring software supports accurate, reliable, and timely patient testing results
- Partner with Operational Excellence to align test strategies with process design, workflow optimization, and scalability initiatives
- Provide input into system requirements and user stories based on laboratory workflow expertise and testing insights
- Support critical feedback loops to ensure continuous improvements to software systems
- Support change management efforts by assessing downstream operational impact of software releases and enhancements
Requirements:
- Bachelor's degree in a scientific discipline (e.g., Biology, Molecular Biology, Bioinformatics) or related field, or equivalent experience
- 2+ years of experience in software testing, quality assurance, or validation, preferably in a regulated environment
- Familiarity with NGS workflows and/or clinical laboratory operations (CLIA, CAP, or equivalent)
- Experience writing and executing test cases based on requirements and specifications
- Strong attention to detail and ability to identify edge cases and failure modes
- Excellent documentation skills with a focus on clarity, completeness, and compliance
- Demonstrated ability to translate complex operational workflows into structured test scenarios and validation strategies
- Experience testing LIMS, LIS, or other laboratory software systems
- Knowledge of software development lifecycle (SDLC) and validation frameworks (e.g., CSV, GxP)
- Experience working in high-complexity molecular diagnostics or MRD testing environments
- Familiarity with data validation, NGS file formats (e.g., FASTQ, BAM, VCF), and/or bioinformatics pipelines
- Exposure to test automation tools or scripting (e.g., Python, SQL)
- Experience working cross-functionally with engineering, bioinformatics, and quality teams
- Exposure to regulated change control processes and software impact assessments in regulated environments