The opportunity
Natera™ is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. Our mission 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 help lead to longer, healthier lives.
What you'll do
Collaborate closely with the Natera QA team to maintain and follow the: Quality Management System (QMS), ensuring Scientific Operations operates in full alignment with company-wide quality standards.
Lead the design and improvement of QA/QC processes across Scientific: Operations; identify gaps in existing systems and implement practical, scalable solutions.
Propose and drive continuous improvements to existing quality workflows,: recommending changes that strengthen compliance without disrupting scientific operations.
Serve as the primary QA contact within Scientific Operations, connecting: closely with the Natera QA team and providing guidance on quality language, standards, and interpretation.
Lead Root Cause Analysis (RCA) and CAPA processes for quality deviations, non-conformances, or audit findings.
Train Scientific Operations staff on QA/QC expectations, documentation standards, and regulatory requirements.
What they're looking for
- Conduct systematic spot-checks and routine audits of lab run packages, sample: logs, and experimental records across Scientific Operations, including both Sample Management and Sample Operations.
- Manage the full lifecycle of SOPs, technical protocols, equipment calibration: logs, and safety documents, including version control and periodic review cycles.
- Support internal and external audit readiness by maintaining organized,: traceable, and audit-ready documentation systems.
- Flag non-compliant or incomplete documentation; work directly with lab staff: and management to resolve gaps and implement corrective actions.