
Associate Scientist I
Green Oaks, ILContract$24–28/hrSeen 1 day agoSeen in employer's feed 1 day ago
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Job overview
The Associate Scientist I will support testing and evaluation of new Transfusion Medicine products in a laboratory, adhering to Good Laboratory Practice, following precise protocols, and generating accurate data for FDA regulatory submissions in a fast‑paced, regulated environment.
Skills & qualifications
Skills
Qualifications
Full 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?
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Perform laboratory testing of new Transfusion Medicine products, assays, and instrumentation.
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Execute studies according to established protocols and Good Laboratory Practice (GLP) requirements.
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Generate, document, and maintain accurate study data and records.
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Support data collection activities for FDA regulatory submissions.
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Complete laboratory documentation and reporting with a high degree of accuracy and attention to detail.
What's Needed?
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Bachelor's degree in a scientific discipline required.
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1-2 years of laboratory experience preferred; strong entry-level candidates will also be considered.
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Understanding of Good Laboratory Practice (GLP).
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Strong attention to detail and documentation skills.
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Ability to follow protocols and maintain accurate records.
What's in it for me?
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Hands-on laboratory experience supporting critical Transfusion Medicine product development.
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Opportunity to contribute study data that supports regulatory submissions and FDA approval processes.
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Structured work focused on protocol execution, documentation accuracy, and quality awareness.
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Clear balance of laboratory work and documentation (approximately 75% laboratory-based activities and 25% documentation/administrative tasks).
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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!
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.
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