Quality Lab Associate

Date Posted: 12/08/2025

Hiring Organization: Rose International

Position Number: 494318

Industry: Healthcare

Job Title: Quality Lab Associate

Job Location: Round Lake, IL, USA, 60073

Work Model: Onsite

Shift: M-F First Shift

Employment Type: Temporary

FT/PT: Full-Time

Estimated Duration (In months): 7

Min Hourly Rate($): 35.26

Max Hourly Rate($): 37.87

Must Have Skills/Attributes: Analysis, Biological testing, Laboratory

Experience Desired: Laboratory experience (2-5 yrs); Experience conducting biological or chemical analysis (2-5 yrs)

Required Minimum Education: Bachelor’s Degree

**C2C is not available**

Requirements

Job Description

• Bachelors Degree in Chemistry, or Biological Science with Analytical Chemistry
• 2-5 years of laboratory experience
• Experience conducting biological or chemical analysis
• Proficient in wet and instrumental methods of analysis.
• Advanced laboratory skills, basic knowledge of statistical methods.
• Strong technical problem-solving skills.
• Ability to handle multiple tasks concurrently, and in a timely fashion.
• Computer literate.
• Must be able to communicate effectively with supervisors and peers.
• Must demonstrate effectiveness in the ability to train others, empowerment, leadership, results orientation and task completion.
  
  

Job Duties

• Conduct critical biological, chemical, and physical analyses on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility.
• Review test data, which includes overall documentation practices.
• Perform release functions in LIMS or other computerized systems.
• Use sophisticated laboratory instrumentation and computer systems to collect and record data.
• Perform advanced biological and chemical assays requiring precise analytical skills and understanding of biology and chemistry principles.
• Complete all testing, including special project/protocol testing in a timely and appropriate manner.
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
• Investigate deviations and write exception documents.
• Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
• Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
• Perform equipment maintenance and calibrations as required.
• **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
• **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
  
  

Benefits

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).