Valencia Medical Lab Technician - Data-Driven Impact

IQVIA

Valencia

Presencial

VES 35.085.000 - 72.966.000

Jornada completa

14 días+
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Descripción de la vacante

IQVIA Laboratories in Valencia, CA is hiring a Medical Lab Technician (MLT) to perform routine analyses and support day-to-day testing in a fast-paced clinical environment.

The role requires a bachelor’s degree in a clinical laboratory science field or equivalent experience, proficiency with lab techniques, and knowledge of GLP standards. The schedule is Tue–Sat, 2:00 PM–10:30 PM, with opportunities to contribute to quality improvements and data management.

Formación

  • Bachelor’s degree in chemical, physical, biological, or clinical laboratory science or equivalent experience.
  • Proficiency with routine laboratory techniques and equipment.
  • Working knowledge of GLP or other applicable regulatory standards.
  • Ability to perform laboratory calculations including averages, means, standard deviations, and QC metrics.
  • Equivalent education/experience may be considered in lieu of degree.

Responsabilidades

  • Perform and document analytical laboratory procedures in compliance with SOPs and regulatory guidelines.
  • Conduct routine data analysis and assess results for accuracy and expected performance.
  • Escalate unusual findings or potential errors to senior laboratory staff.
  • Prepare and upload data analysis results to the LIMS system under guidance.
  • Support quality investigations, deviations, and process improvements.

Conocimientos

Lab techniques
Data analysis
GLP knowledge
Attention to detail

Educación

Bachelor's degree in clinical lab science

Herramientas

LIMS
Spectrophotometer

Descripción del empleo

IQVIA Laboratories in Valencia, CA is hiring a Medical Lab Technician (MLT) to perform routine analyses and support day-to-day testing in a fast-paced clinical environment.

The role requires a bachelor’s degree in a clinical laboratory science field or equivalent experience, proficiency with lab techniques, and knowledge of GLP standards. The schedule is Tue–Sat, 2:00 PM–10:30 PM, with opportunities to contribute to quality improvements and data management.

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