Laboratory Associate

IQVIA; California; On-site; USD 36,000 - 75,000; Full time

Job summary

IQVIA Laboratories in Valencia, CA is hiring a Lab Associate to perform routine hematology testing for clinical trials. You will handle specimen testing, data review, documentation, and support regulatory compliance while contributing to continuous improvement.

Requirements include a High School Diploma or Bachelor's degree with at least 6 months of lab experience, knowledge of GLP and SOPs, and the ability to follow procedures, document results, and collaborate with cross-functional teams.

Qualifications

• High School Diploma or Bachelor's Degree with 6 months lab experience
• Knowledge of GLP, SOPs, and regulatory standards
• Ability to document results and follow procedures with attention to detail

Responsibilities

• Perform routine analysis of specimens and document results per SOPs and guidelines
• Evaluate results against lab system algorithms and identify discrepancies
• Escalate unusual findings to senior personnel
• Prepare buffers, solutions, and materials for testing
• Store samples and reagents properly after testing
• Assist with procedure development and continuous improvement
• Support housekeeping, safety, and 6S initiatives
• Communicate with cross-functional stakeholders and notify staff of supply shortages

Skills

GLP knowledge

SOP compliance

Laboratory equipment knowledge

Communication skills

Attention to detail

Education

High School Diploma

Bachelor's Degree in Chemistry/ Biology/ Medical Laboratory Technology

Tools

Laboratory instrumentation

Computer skills

Job description

## Laboratory AssociateApplylocations: Valencia, CA, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1560780## We are seeking Lab Associate join IQVIA Laboratories at Valencia, CA.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. **Schedule: There are multiple shifts time available**### Job Summary:Perform routine hematology laboratory testing and analysis to generate accurate data for clinical trials research. This role is responsible for specimen testing, data review, documentation, laboratory support activities, and maintaining compliance with applicable regulatory and quality standards.### What You'll Be Doing:* Perform routine analysis of specimens and document results in accordance with SOPs and regulatory guidelines* Evaluate analytical results against laboratory system algorithms and identify discrepancies* Escalate unusual findings, performance issues, or potential errors to senior laboratory personnel* Prepare buffers, solutions, and materials required for laboratory testing* Store samples and reagents appropriately following analysis activities* Assist with laboratory procedure development, documentation updates, and continuous improvement efforts* Support laboratory housekeeping, safety, quality, and 6S initiatives* Communicate effectively with cross-functional stakeholders and notify staff of supply shortages### What We Are Looking For:* High School Diploma or equivalent **OR** Bachelor's Degree (some CAP/CLIA laboratory locations may require a BS in Chemistry, Biology, or Medical Laboratory Technology) 6 months relevant lab experience* Basic knowledge of laboratory principles* Basic knowledge of Good Laboratory Practices (GLP) and applicable regulatory agency standards* Knowledge of laboratory equipment, instrumentation, and terminology used within the area of responsibility* Knowledge of laboratory safety, infection control procedures, standard precautions, and hazardous chemical handling* Applicable certifications and licenses as required by country, state, and/or other regulatory bodies* Other equivalent combination of education, training, and experience may be accepted in lieu of degree### The Knowledge, Skills and Abilities Needed for This Role:* Ability to maintain effective reporting procedures and control workflow* Ability to effectively collaborate with internal stakeholders* Basic computer skills and attention to detail when documenting analytical results* Strong organizational and communication skills* Ability to follow SOPs and regulatory requirements consistently### Physical Demands: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.### What We Offer You:We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.To learn more about our benefits, visit IQVIA Benefits.If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $35,900.00 - $74,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.