Quality Lab Associate

at Rose International Inc. in Round Lake, Illinois, United States

Job Description

Date Posted: 04/12/2024

Hiring Organization: Rose International

Position Number: 462226

Job Title: Quality Lab Associate

Job Location: Hainesville, IL, USA, 60073

Work Model: Onsite

Employment Type: Temporary

Estimated Duration (In months): 13  

Min Hourly Rate($): 24.00  

Max Hourly Rate($): 27.00

Must Have Skills/Attributes: Quality Analyst

Job Description

**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.**

Education and/or Experience. 0 N/A: Intern or Co-op
• Bachelor’s degree in Chemistry or biological science with analytical chemistry laboratory coursework and 0-1 years’ experience.
• Analytical chemistry instrumentation experience (e.g. HPLC, pH, KF, AA, GFAA, titrations, etc.) preferred.
• Pharmaceutical GMP/QC laboratory experience is desired.

Summary:
The position may be responsible for analytical testing, validation/verification, and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake, IL Stability Laboratories within Product Quality serving multiple global businesses.
This role is essential for supporting the global commercial product teams and/or product development teams. The position may interface with multiple functions. The individual in this position must: 1) Effectively demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance. 2) Display basic technical understanding of related disciplines. 3) Conduct routine/non-routine experiments with minimal assistance.
A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials.

Essential Duties and Responsibilities:
• Under direction, conduct critical chemical, physical, and biological analyses on finished product stability samples. May also support testing of raw materials, initial, in-process and final product samples from the manufacturing facility, as required. Work under minimum supervision.
• Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to conduct validations.
• Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules.
• Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
• Participate with management to investigate deviations and write exception documents.
• May perform advanced biological and chemical assays requiring precise analytical skills and understanding of chemistry principles.
• May perform review of test data, which includes overall documentation practices. May perform review functions in LIMS or other computerized systems.
• May participate in cross functional teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality and provide new product support.
• Maintain laboratory supplies and laboratory safety requirements to ensure audit readiness at all times.
• Perform equipment maintenance and calibrations as required. Troubleshoot and resolve instrument problems with some assistance.

Qualifications:
• Proficient in advanced wet chemistry, volumetric preparation techniques and instrumental methods of analysis
• Must demonstrate effectiveness in attention to detail, organization, teamwork/interpersonal skills, results orientation, and task completion.
• Must be able to handle multiple tasks concurrently and in a timely fashion.
• Possess writing and computer skills.
• Must communicate effectively with managers and peers.
• Interpret available information and make recommendations to resolve technical challenges.

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.).