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IQVIA

Runs drug trials and sells health data to pharma

Laboratory Associate - Flow Cytometry

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeValencia, Santa Clarita, CA, USAIn-person

About the Job

Requirements

  • A bachelor's degree or equivalent combination of education and experience is required. Some CAP/CLIA lab locations may require a Bachelor of Science in chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology.
  • Six months of experience in a regulated laboratory environment is preferred.
  • Basic knowledge of the assigned technical area, systems, and procedures obtained through prior work experience.
  • Understanding of the functional area and its responsibilities.
  • Working knowledge of applicable regulatory standards within the area of responsibility, such as Good Laboratory Practices.
  • 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 for batches and specimens, including averages, means, standard deviations, and quality control metrics.
  • Computer skills using Microsoft Outlook, Word, and Excel.
  • Ability to handle multiple tasks simultaneously.
  • Attention to detail and accuracy.
  • Ability to collaborate with internal stakeholders.

Responsibilities

  • Perform and document analytical procedures in accordance with standard operating procedures and regulatory guidelines.
  • Perform routine data analysis to determine whether an analytical procedure is proceeding as expected and results are within acceptable tolerances.
  • Identify and document potential performance errors or unusual results and escalate them to senior laboratory personnel.
  • Prepare data analysis results for upload to the laboratory information management system under the guidance of senior staff.
  • Assist with quality investigations, deviations, and resolution.
  • Prepare buffers and solutions for analysis 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.
  • Perform and document hands-on training for other laboratory personnel in areas of proven competency as assigned.
  • Assist in reviewing and developing laboratory procedures and techniques.
  • Assist in implementing procedural changes as assigned.
  • Notify inventory staff of supply shortages.
  • Represent the laboratory team on cross-functional projects as needed.
  • Communicate clearly, accurately, and promptly 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.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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