Molecular Lab Technologist II (CLIA/QC)

Precision Medicine Group

Houston (TX)

On-site

USD 46,000 - 68,000

Full time

7 days ago
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Job summary

Precision Medicine Group in Houston seeks a Technologist II (Molecular) to advance molecular biology assays from development to execution. You will train staff, run QC and clinical samples, and help maintain SOPs under CLIA/GLP/GCP standards.

You will collaborate with scientists, manage reagents, and perform routine instrument maintenance while supporting process improvements and regulatory documentation.

Qualifications

  • Bachelor’s Degree in Life Sciences or related discipline.
  • 2+ years of related laboratory experience.
  • Must be able to work evenings/weekends/holidays as needed.
  • Strong computational skills (Word, Excel, PowerPoint, etc.).

Responsibilities

  • Perform assays according to SOPs and support assay development.
  • Train staff on project-related assays and SOPs.
  • Run quality control samples and clinical samples; generate data.
  • Maintain reagents and consumables stock.
  • Perform instrument maintenance and troubleshooting.
  • Collaborate with scientists on assay qualification for new projects.
  • Ensure documentation supports CLIA/GLP/GCP standards.
  • Coordinate freezer transfers and quality control entries.
  • Contribute to cross-functional process improvements.
  • Other duties as assigned.

Skills

Molecular biology techniques
RNA/DNA extraction
qPCR
NGS
Quality control
Data analysis
Lab equipment maintenance
Shift work
Staff training
Regulatory knowledge (CLIA/GLP/ISO)
Document control

Education

Bachelor's Degree in Life Sciences / Biology or related

Job description

Precision Medicine Group in Houston seeks a Technologist II (Molecular) to advance molecular biology assays from development to execution. You will train staff, run QC and clinical samples, and help maintain SOPs under CLIA/GLP/GCP standards.

You will collaborate with scientists, manage reagents, and perform routine instrument maintenance while supporting process improvements and regulatory documentation.

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