Lab Associate

IQVIA•Santa Clarita, CA

19h•Onsite

About The Position

We are seeking a Lab Associate to join IQVIA Laboratories at Valencia. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. This role is responsible for performing routine testing procedures on specimens to generate data supporting clinical trials research, ensuring results are documented accurately and in compliance with SOPs and applicable regulatory guidelines.

Requirements

Minimum Education: High School Diploma or equivalent, or Bachelor’s Degree (some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology)
Experience working in a laboratory environment performing routine testing procedures (minimum 6 months or equivalent combination of training and experience)
Basic knowledge of Good Laboratory Practices (GLP) and applicable regulatory standards, including laboratory safety and infection control procedures
Other Equivalent combination of education, training, and experience may be accepted in lieu of degree
Working knowledge of laboratory equipment, basic instrumentation, and terminology used in the assigned area
Ability to maintain accurate documentation, follow established workflows, and support effective reporting procedures
Basic computer skills and ability to evaluate results using laboratory computer systems
Ability to collaborate effectively with internal stakeholders and communicate clearly and professionally
Commitment to safety, quality, and 6S initiatives and adherence to procedures and regulatory requirements
Ability to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints).
Physical demands vary depending on assigned work area and work tasks.
Occasional exposure to cold temperatures.

Responsibilities

Perform routine specimen testing and document results in accordance with SOPs and applicable regulatory guidelines
Evaluate analytical result validity against laboratory computer system algorithms and established criteria
Identify, document, and escalate potential performance errors or unusual results to senior laboratory personnel
Prepare buffers and solutions required for testing and analysis
Store post-analysis samples and reagents according to defined requirements
Support laboratory housekeeping activities consistent with 6S standards
Notify appropriate staff of supply shortages and support inventory awareness
Communicate clearly and timely with cross-functional stakeholders and participate in continuing education activities