Back to results

Associate Scientist I

  • Green Oaks, IL, United States

$24 to $28 USD / hour

Applications open in a new tab.

Job details

Pay
$24 to $28 USD / hour
Apply by
Education
Bachelor’s degree
Posting language
English
Posted

Original job description

Our client, a leader in Transfusion Medicine product development, is seeking an Associate Scientist I to join their team. As an Associate Scientist I, you will support the testing and evaluation of new Transfusion Medicine products in a laboratory environment. The ideal candidate will bring a strong commitment to Good Laboratory Practice (GLP), a drive to follow protocols with precision, and the motivation to learn quickly in a fast-paced, regulated setting - all while contributing data that supports regulatory submissions and FDA approval processes. Title: Associate Scientist I Location: Abbott Park, Illinois Duration: 12+ Month contract Pay Range: $24/hr. - $28/hr. Must be flexible to work 7:00 AM - 3:00 PM, 10:00 AM - 6:00 PM, or 2:00 PM - 10:00 PM. Shift assignments may change with two weeks' notice. Saturday required 1-2 times per month: 8:00 AM - 2:30 PM.

What's the Job?

  • Perform laboratory testing of new Transfusion Medicine products, assays, and instrumentation.
  • Execute studies according to established protocols and Good Laboratory Practice (GLP) requirements.
  • Generate, document, and maintain accurate study data and records.
  • Support data collection activities for FDA regulatory submissions.
  • Complete laboratory documentation and reporting with a high degree of accuracy and attention to detail. What's Needed?
  • Bachelor's degree in a scientific discipline required.
  • 1-2 years of laboratory experience preferred; strong entry-level candidates will also be considered.
  • Understanding of Good Laboratory Practice (GLP).
  • Strong attention to detail and documentation skills.
  • Ability to follow protocols and maintain accurate records. What's in it for me?
  • Hands-on laboratory experience supporting critical Transfusion Medicine product development.
  • Opportunity to contribute study data that supports regulatory submissions and FDA approval processes.
  • Structured work focused on protocol execution, documentation accuracy, and quality awareness.
  • Clear balance of laboratory work and documentation (approximately 75% laboratory-based activities and 25% documentation/administrative tasks).
  • A fast-paced environment where adaptability and quick learning are valued. If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
More about this job

Skills

  • Good laboratory practice
  • Good laboratory practices
  • Abbott
  • Perform laboratory tests
  • Documentation
  • Reporting
  • Attention to detail
  • Adaptability

Report this job