Lab Associate - Flow Cytometry

IQVIASanta Clarita, CA
1dOnsite

About The Position

We are seeking a Laboratory Associate- Flow Cytometry to join IQVIA’s laboratory business at Valencia, CA. Shift: Saturday-Wednesday, 4PM - 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.

Requirements

  • 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.
  • 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.

Nice To Haves

  • 6 months experience in a regulated laboratory environment.

Responsibilities

  • performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines
  • performing routine data analysis
  • identifying and documenting potential performance errors
  • preparing data analysis results for upload to LIMS system
  • assisting in quality investigations, deviations, and resolution
  • preparing buffers and solutions for analysis, as required
  • assisting in the review and update of laboratory procedures and techniques
  • guiding entry level staff on routine procedures and supports on-boarding of new staff
  • performing and documenting calibration and maintenance of laboratory equipment as assigned
  • performing and documenting hands on training for other lab personnel in areas of proven competency as assigned
  • assisting in the review and development of laboratory procedures and techniques
  • assisting in the implementation of procedural changes as assigned
  • notifying inventory staff of supply shortages
  • representing lab team on cross functional projects
  • clear, accurate, and timely communications with cross functional stakeholders
  • participating in continuing education through self-study, attending training sessions and lectures and meetings
  • supporting safety, quality, and 6S requirements and initiatives
  • complying with company's procedures and applicable regulatory requirements

Benefits

  • 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.
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