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Genomic Test Kit Processor

Job

The Start Center for Cancer Care

San Antonio, TX (In Person)

Full-Time

Posted 4 days ago (Updated 8 hours ago) • Actively hiring

Expires 6/22/2026

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Job Description

Genomic Test Kit Processor The Start Center for Cancer Care - 2.9 San Antonio, TX Job Details Full-time 1 day ago Qualifications High school diploma or GED Full Job Description Why Join Us? The START Center is growing! We are pioneering premier Cancer Care for our patients with leading doctors, advanced diagnostics and cutting-edge therapies. We offer competitive wages, benefits, and yearly bonus opportunities. The growth of our organization and our innovative environment to treat and care for patients that have cancer make us a great match for anyone looking to begin or further their career at a company with a mission that truly impacts lives.
Job Description:
Genomic Test Kit Processor Position Summary The Genomic Test Kit Processor is responsible for receiving, verifying, and preparing genomic testing kits for laboratory analysis. This role ensures that all incoming specimens are accurately logged, properly handled, and processed according to established protocols to maintain sample integrity and support high‑quality genetic testing outcomes. Key Responsibilities Receive and log incoming genomic test kits , verifying patient information, requisition forms, and kit completeness. Inspect samples for compliance with collection, labeling, and transport requirements; identify and escalate discrepancies. Prepare specimens for laboratory workflows , including accessioning, barcoding, aliquoting, and organizing samples for downstream testing. Maintain chain‑of‑custody documentation and ensure accurate data entry into the laboratory information management system (LIMS). Follow strict biosafety and quality control procedures to protect sample integrity and maintain regulatory compliance (CLIA, CAP, HIPAA). Coordinate with laboratory staff to prioritize urgent or time‑sensitive samples. Monitor inventory of test kits, reagents, and processing supplies; report shortages or issues. Support continuous improvement efforts by identifying workflow inefficiencies and recommending process enhancements. Maintain a clean, organized, and compliant work environment in accordance with laboratory safety standards. Research data in the EMR, Electronic Medical Record, system Qualifications High school diploma or equivalent required; associate or bachelor's degree in biology, biotechnology, or related field preferred . Experience in a clinical, research, or diagnostic laboratory setting is highly desirable. Strong attention to detail and ability to follow precise protocols. Comfortable working with biological specimens and adhering to biosafety guidelines. Proficient with data entry and basic computer systems; experience with LIMS is a plus. Ability to work efficiently in a fast‑paced, high‑volume environment. Strong communication and teamwork skills. Physical & Work Environment Requirements Ability to stand for extended periods and perform repetitive tasks. Ability to lift up to 25 lbs. Work performed in a laboratory environment with exposure to biological materials and chemicals.

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