
51 - 200 employees
Founded 2009
🧬 Biotechnology
☁️ SaaS
🤝 B2B
Biotechnology • SaaS • B2B
Genista Biosciences is a Silicon Valley–based laboratory testing company that combines robotics, automation, proprietary software, and molecular techniques (real-time PCR and next‑generation sequencing) to deliver fast, accredited food-safety, microbiological, chemical, contaminant, pesticide, mycotoxin, allergen, and GMO testing. The company provides next‑day turnaround, an online platform for sample submission and results tracking, and serves manufacturers, CPG brands, growers, and bio-pharma/supplement customers with ISO 17025–accredited methods and built‑in quality controls to reduce costs and improve accuracy.
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51 - 200 employees
Founded 2009
🧬 Biotechnology
☁️ SaaS
🤝 B2B
Biotechnology • SaaS • B2B
Genista Biosciences is a Silicon Valley–based laboratory testing company that combines robotics, automation, proprietary software, and molecular techniques (real-time PCR and next‑generation sequencing) to deliver fast, accredited food-safety, microbiological, chemical, contaminant, pesticide, mycotoxin, allergen, and GMO testing. The company provides next‑day turnaround, an online platform for sample submission and results tracking, and serves manufacturers, CPG brands, growers, and bio-pharma/supplement customers with ISO 17025–accredited methods and built‑in quality controls to reduce costs and improve accuracy.
• Review analytical data generated from LC-MS/MS, GC-MS/MS, ICP-MS, HPLC, and GC methods for accuracy, completeness, and compliance. • Perform and document Out-of-Specification (OOS) and Out-of-Trend (OOT) investigations. • Conduct root cause analysis and implement corrective and preventive actions (CAPA) as required. • Evaluate quality control results, calibration data, system suitability, and method performance. • Troubleshoot analytical instrumentation and analytical issues impacting data quality. • Review and approve laboratory worksheets, calculations, chromatograms, spectra, and final reports. • Assist with method validation, verification, and transfer. • Ensure compliance with ISO 17025, GMP, GLP, and internal quality requirements. • Investigate deviations and support laboratory quality assurance activities. • Maintain accurate documentation and ensure data integrity requirements are met.
• Master's with 4+ years of experience in an analytical testing laboratory post qualification or Ph.D. degree with 2+ years of experience post qualification • Strong understanding of chromatographic and mass spectrometric techniques including: LC-MS/MS, GC-MS/MS, ICP-MS, HPLC/UHPLC, GC • Working knowledge of ISO 17025, GMP, GLP, and laboratory quality systems
• Fully Remote
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