Lab Associate Flow Cytometry

IQVIA Inc; California; On-site; USD 35,000 - 72,000; Full time

Job summary

IQVIA Inc. in Valencia, CA is seeking a Laboratory Associate- Flow Cytometry to join our laboratory team. The role focuses on performing analytical procedures, data analysis, and calibration under SOPs and GLP guidelines.

You will train entry-level staff, support quality investigations, and maintain equipment while communicating with cross-functional partners. Shift: Tuesday to Saturday, 4 PM to 12:30 AM; full-time.

Qualifications

• Bachelor's degree or higher in a chemical, physical, biological or clinical laboratory science, medical laboratory technology or cytotechnology.
• 6 months experience in a regulated laboratory environment.
• Knowledge of GLP and regulatory standards.
• Proficiency with routine laboratory calculations (averages, means, SD).
• Strong computer skills (Outlook, Word, Excel).
• Ability to collaborate with internal stakeholders.

Responsibilities

• Perform and document analytical procedures per SOPs and regulatory guidelines.
• Analyze data to ensure results are within expected tolerances.
• Escalate performance issues to senior staff.
• Prepare data for upload to LIMS under guidance of seniors.
• Assist in quality investigations and deviations.

Skills

Bachelor's degree

Regulated lab exp

GLP knowledge

MS Excel/Outlook

Attention to detail

Cross-functional collaboration

Education

Bachelor's degree

Tools

LIMS

Job description

Valencia, CA, United States of America

Full time

R1535921

We are seeking a Laboratory Associate- Flow Cytometry to join IQVIA’s laboratory business at Valencia, CA.

Shift: Tuesdays 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, visithttps://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.com

IQVIA 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/eoe

IQVIA 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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