Lab Associate - Flow Cytometry
IQVIA, Santa Clarita, CA, United States
We are seeking a Laboratory Associate – Flow Cytometry to join IQVIA’s laboratory business at Valencia, CA.
About the Role
Shift: Tuesday to Saturday 4PM to 12:30 AM
Responsibilities
Perform and document analytical procedures in accordance with SOPs and regulatory guidelines.
Conduct routine data analysis to verify procedures are proceeding correctly and results are within acceptable tolerances.
Identify and document potential performance errors or unusual results and escalates them to senior lab personnel.
Prepare data analysis results for upload to the LIMS system under guidance of senior staff.
Assist in quality investigations, deviations, and resolution.
Prepare buffers and solutions as required.
Assist in reviewing and updating laboratory procedures and techniques.
Guide entry‑level staff on routine procedures and support onboarding of new staff.
Perform and document calibration and maintenance of laboratory equipment as assigned.
Provide hands‑on training for other lab personnel in areas of proven competency as assigned.
Assist in implementation of procedural changes as assigned.
Notify inventory staff of supply shortages.
May represent the lab team on cross‑functional projects.
Communicate clearly, accurately, and timely with cross‑functional stakeholders.
Participate in continuing education through self‑study, training sessions, lectures, and meetings.
Support safety, quality, and 6S requirements and initiatives.
Comply with company procedures and applicable regulatory requirements.
Qualifications
Bachelor’s Degree or equivalent combination of education and experience. (Some CAP/CLIA lab locations may require a BSc in a chemical, physical, biological or clinical laboratory science, medical laboratory technology, or cytotechnology.)
Minimum 6 months experience in a regulated laboratory environment.
Required Skills
Basic knowledge of the assigned technical area, systems and procedures obtained through prior work experience.
Demonstrated understanding of the functional area and responsibilities.
Working knowledge of applicable regulatory standards 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.
Capability to handle multiple tasks simultaneously.
Strong attention to detail and accuracy.
Ability to collaborate effectively with internal stakeholders.
Equal Opportunity Statement
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
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About the Role
Shift: Tuesday to Saturday 4PM to 12:30 AM
Responsibilities
Perform and document analytical procedures in accordance with SOPs and regulatory guidelines.
Conduct routine data analysis to verify procedures are proceeding correctly and results are within acceptable tolerances.
Identify and document potential performance errors or unusual results and escalates them to senior lab personnel.
Prepare data analysis results for upload to the LIMS system under guidance of senior staff.
Assist in quality investigations, deviations, and resolution.
Prepare buffers and solutions as required.
Assist in reviewing and updating laboratory procedures and techniques.
Guide entry‑level staff on routine procedures and support onboarding of new staff.
Perform and document calibration and maintenance of laboratory equipment as assigned.
Provide hands‑on training for other lab personnel in areas of proven competency as assigned.
Assist in implementation of procedural changes as assigned.
Notify inventory staff of supply shortages.
May represent the lab team on cross‑functional projects.
Communicate clearly, accurately, and timely with cross‑functional stakeholders.
Participate in continuing education through self‑study, training sessions, lectures, and meetings.
Support safety, quality, and 6S requirements and initiatives.
Comply with company procedures and applicable regulatory requirements.
Qualifications
Bachelor’s Degree or equivalent combination of education and experience. (Some CAP/CLIA lab locations may require a BSc in a chemical, physical, biological or clinical laboratory science, medical laboratory technology, or cytotechnology.)
Minimum 6 months experience in a regulated laboratory environment.
Required Skills
Basic knowledge of the assigned technical area, systems and procedures obtained through prior work experience.
Demonstrated understanding of the functional area and responsibilities.
Working knowledge of applicable regulatory standards 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.
Capability to handle multiple tasks simultaneously.
Strong attention to detail and accuracy.
Ability to collaborate effectively with internal stakeholders.
Equal Opportunity Statement
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
#J-18808-Ljbffr