Lab Associate Flow Cytometry

IQVIA; California; Hybrid; USD 35,000 - 72,000; Full time

Job summary

IQVIA in Valencia, CA, is seeking a Laboratory Associate - Flow Cytometry to support analytical testing in a regulated lab environment.

The role includes performing procedures per SOPs, data analysis, preparing buffers, training entry-level staff, and ensuring safety and quality standards while coordinating with cross-functional teams.

You will contribute to calibration, LIMS uploads, and continuous improvement of laboratory procedures in a fast-paced setting.

Qualifications

• Bachelor's degree in chemical, physical, biological or clinical laboratory science or related field.
• 6 months experience in a regulated laboratory environment.
• Knowledge of GLP and laboratory safety practices.

Responsibilities

• Perform and document analytical procedures per SOPs.
• Analyze data to ensure procedures meet expectations within tolerances.
• Prepare data analysis results for upload to LIMS.
• Assist in quality investigations and deviations.
• Calibrate and maintain laboratory equipment as assigned.
• Train entry level staff and support onboarding.

Skills

Regulated lab environment experience

LIMS data handling

Analytical data analysis

Laboratory math calculations

Microsoft Outlook/Word/Excel

Cross-functional collaboration

Education

Bachelor's Degree in lab science or equivalent

Tools

LIMS

Automated lab equipment

Job description

## Lab Associate Flow CytometryApply: Valencia, CA, United States of America: Full time: Posted Yesterday: End Date: September 14, 2026 (2 days left to apply): R1535921We are seekinga **Laboratory Associate- Flow Cytometry** to join IQVIA’s laboratory business at Valencia, CA.**Shift:** **Tuesday to Saturday 4PM to 12:30 AM**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.## **What you’ll be doing:**• Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines. • Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances. • Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel. • Prepares data analysis results for upload to LIMS system under the guidance of senior level staff. • Assists in quality investigations, deviations, and resolution. • Prepares buffers and solutions for analysis, as required. • Assists in the review and update of laboratory procedures and techniques. • Guides entry level staff on routine procedures and supports on-boarding of new staff. • Performs and document calibration and maintenance of laboratory equipment as assigned. • Performs and documents hands on training for other lab personnel in areas of proven competency as assigned. • Assists in the review and development of laboratory procedures and techniques. • Assists in the implementation of procedural changes as assigned. • Notifies inventory staff of supply shortages. • May represent lab team on cross functional projects. • Responsible for clear, accurate, and timely communications with cross functional stakeholders. • Participates in continuing education through self-study, attending training sessions and lectures and meetings. • Supports safety, quality, and 6S requirements and initiatives. • Complies with company's procedures and applicable regulatory requirements.## **The Knowledge, Skills and Abilities needed for this role:*** Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science, medical laboratory technology or cytotechnology.) Req• 6 months experience in a regulated laboratory environment. Pref • Requires basic knowledge of assigned technical area, systems and procedures obtained through prior work experience. • Demonstrates understanding of functional area and responsibilities. • Working knowledge of any applicable regulatory standards within area of responsibility, such as Good Laboratory Practices (GLP). • Proficiency with relevant laboratory techniques. • Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling. • Experience working with automation or specialized laboratory equipment. • Proficiency with routine and some non-routine laboratory calculations regarding batches and specimens including averages, means, standard deviations, and various quality control metrics. • Good computer skills using Microsoft Outlook, Word and Excel. • Capable of handling multiple tasks simultaneously. • Strong attention to detail and accuracy. • Ability to effectively collaborate with internal stakeholders.## **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 https://jobs.iqvia.com/benefits.If you’re looking to unleash your potential, join IQVIA’s laboratory business, 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 $34,700.00 - $72,300.00. 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.