Lab Associate at IQVIA
Singapore, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

07 Nov, 25

Salary

0.0

Posted On

07 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Laboratory Safety, Population Health, Patient Outcomes, Computer Skills, Chemical Handling, Commercialization, Biology, Chemistry, Terminology, Instrumentation, Training, Laboratory Equipment

Industry

Pharmaceuticals

Description

QUALIFICATIONS

  • High School Diploma or equivalent or Bachelor’s Degree. Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree
  • 6 months relevant lab experience or equivalent combination of education, training and experience
  • 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
    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.co
Responsibilities
  • 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.
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