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Quality Laboratory Associate Iii

5+ years
Not Disclosed
10 April 25, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Quality Laboratory Associate III
Req # JR - 167453
Location: Round Lake, Illinois, United States
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Overview

As a member of Baxter's Quality team, you will play an essential role in ensuring the safety of patients by supporting the mission of saving and sustaining lives. Quality is involved in all stages of product development, and this role provides ample growth opportunities while making a daily impact on people’s lives.


Success Profile

What makes a successful Quality team member at Baxter? Here are some key traits:

  • Detail-Oriented

  • Continuous Learner

  • Courageous

  • Collaborative

  • Critical Thinker

  • Influential


Your Role at Baxter

You will be involved in biological, chemical, and physical analyses of pharmaceutical products at various stages of the manufacturing process. You’ll work with raw materials, in-process products, finished goods, and environmental monitoring programs. The role requires working on first shift, with some weekends to support training and projects.


Responsibilities

  • Conduct critical chemical and physical analysis on raw materials and products (initial, in-process, and final).

  • Perform qualification and validation for lab equipment and computer systems.

  • Provide mentorship and training to new hires and junior lab associates.

  • Review test data and documentation to ensure compliance with company standards and regulatory guidelines.

  • Operate sophisticated lab instruments (e.g., HPLC, GC) and computer systems for data collection.

  • Serve as Subject Matter Expert (SME) on equipment troubleshooting and maintenance.

  • Participate in problem-solving teams and improvement projects to enhance quality, production efficiency, and cost savings.

  • Perform laboratory and manufacturing audits as needed.

  • Maintain a clean and organized lab, ensuring compliance with safety regulations and cGMP standards.


Requirements

  • Education: Bachelor's degree in Chemistry or a related field.

  • Experience: At least 5 years in a laboratory setting, with strong technical and analytical skills.

  • Knowledge: Familiarity with cGMP, GLP, FDA, and USP/ICH guidelines preferred.

  • Skills: Ability to mentor, communicate effectively, and handle multiple tasks simultaneously.

  • Physical: Ability to lift up to 50 pounds as needed.

  • Health: Must not be allergic to penicillin, cephalosporins, or related products.

  • Weekend Availability: Occasional weekend work required.


Compensation

The estimated base salary for this role is between $80,000 and $110,000 annually, with potential bonuses. Actual pay will depend on experience, location, and other factors.


Benefits

Baxter offers a comprehensive benefits package, including health, dental, and vision coverage starting on day one, as well as paid time off, paid parental leave, a 401(k) plan, and more.


Equal Employment Opportunity

Baxter is an equal opportunity employer, evaluating applicants without regard to race, gender, sexual orientation, or other legally protected characteristics.