Clinical genomics lab scaling precision diagnostics across 50 states
Baylor Genetics operates a large clinical genomics lab (501–1,000 employees) built on a polyglot data stack—SQL, Python, R, TensorFlow, Hugging Face, and cloud infrastructure (Azure, AWS, GCP)—processing whole-genome and whole-exome sequencing across family planning, oncology, and rare-disease testing. Hiring is accelerating across healthcare, sales, and research roles, with notable leadership focus on clinical operations, market access, and regulatory compliance, signaling active scaling in both testing volume and reimbursement pathways.
Notable leadership hires: Compliance Director, Clinical Director, Market Access Director
Baylor Genetics is a diagnostic genomics laboratory headquartered in Houston's Texas Medical Center, serving clinicians and patients across 50 U.S. states. The company offers a full menu of genetic testing—including whole-genome sequencing, whole-exome sequencing, and focused diagnostic panels—alongside genetic counseling to guide medical management and reduce diagnostic delay for rare and complex disorders. Core test areas span reproductive carrier screening, prenatal and neonatal diagnostics, pediatric genetics, and oncology. The organization combines clinical laboratory operations with data analysis and assay development to maintain test quality and turnaround time.
Baylor Genetics runs Python, R, C++, TensorFlow, and Hugging Face for data analysis, with SQL/PostgreSQL/MongoDB for data management and cloud infrastructure on Azure, AWS, and GCP for compute and storage.
Yes. Active hiring spans 121 total roles, including engineering (14 open), data (6 open), and research (16 open), with seniority distribution tilted toward senior and director-level positions.
Baylor Genetics provides whole-genome sequencing, whole-exome sequencing, reproductive carrier screening, prenatal/neonatal testing, pediatric genetics, oncology diagnostics, and rare-disease panels, supported by genetic counselors across 50 U.S. states.
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