Laboratory Associate 1 - PBMC Tech at IQVIA Nordic

Job Overview

Responsible for performing a variety of routine testing procedures to obtain
data for use in clinical trials research.


  • Performs routine analysis of specimens and documents results in accordance with SOPs and applicable regulatory guidelines.
  • Evaluates validity of analytical results against the algorithms displayed by the lab computer system.
  • Identifies and documents potential performance errors or otherwise unusual results and escalate to senior lab personnel.
  • Responsible for preparation of buffers and solutions for analysis, as required.
  • May perform secondary review of analytical results when signed-off as competent to do so for applicable instrument(s) and/or data type(s).
  • Responsible for post analysis sample and reagent storage.
  • Assists in the development and writing of new laboratory procedures and techniques.
  • Assists in good housekeeping of the lab environment, consistent with 6S standards.
  • Notifies appropriate staff of supply shortages.
  • Responsible for clear, accurate, and timely communications with cross functional stakeholders.
  • Participates in continuing education through self-study, attending in-services and lectures and meetings.
  • Supports safety, quality, and 6S requirements and initiatives.
  • Complies with company's procedures and applicable regulatory requirements.

  • High School Diploma or equivalent required
  • 6 months relevant lab experience required or
  • Equivalent combination of education, training and experience required

  • Basic knowledge of lab principles.
  • Basic knowledge of Good Laboratory Practices (GLP) and applicable regulatory agency standards.
  • Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.
  • Knowledge of laboratory equipment, instrumentation and terminology used in the area of responsibility.
  • Basic computer skills.
  • Ability to maintain effective reporting procedures and control workflow.
  • Ability to effectively collaborate with internal stakeholders.
  • Applicable certifications and licenses as required by country, state, and/or other regulatory bodies required

Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions.
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status.

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