Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Quality Lab Associate I -1st Shift (Monday-Friday)

0.6-1 years
USD 64,000 – 88,000
10 Dec. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 Lab Associate I – 1st Shift (Monday–Friday)

Req ID: JR-192163
Location: Round Lake, Illinois, United States

Overview

Baxter is a global leader in healthcare, dedicated to delivering products and technologies that save and sustain lives. As part of the Quality team, you will contribute directly to patient safety and product reliability across the complete product lifecycle. Quality roles at Baxter offer significant opportunities for professional development, continuous learning, and long-term career growth in a highly regulated environment.

Position Summary

The Quality Lab Associate I is responsible for performing biological, chemical, and physical analyses on pharmaceutical products throughout the manufacturing cycle, including raw materials, in-process samples, final products, and environmental monitoring samples. This is a full-time, on-site 1st shift role (Monday–Friday).

Candidates must not be allergic to Penicillin, Cephalosporin, or related compounds.

Key Responsibilities

  • Perform chemical and physical testing on raw materials, in-process samples, and finished products, as well as environmental monitoring samples.

  • Operate analytical laboratory instruments such as HPLC, FTIR, UV-Vis, and GC, and manage data collection through computerized systems.

  • Conduct advanced analytical assays requiring strong understanding of chemistry, biology, and laboratory best practices.

  • Ensure compliance with FDA, GLP, QSR, cGMP standards, and Baxter SOPs while maintaining high standards of data integrity.

  • Participate in team-based problem-solving initiatives to support production, improve efficiency, and enhance product quality.

  • Conduct laboratory and manufacturing audits; revise SOPs as needed.

  • Perform routine equipment calibration and maintenance.

  • Document all testing activities accurately in notebooks, LIMS, controlled forms, and other quality systems.

  • Maintain a clean, safe, and compliant laboratory environment.

  • Investigate deviations and prepare associated documentation, including OOL, OOS, OOT, and exception reports.

  • Support continuous improvement initiatives using Lean principles such as 6S and Kaizen.

  • Communicate proactively with team members and management regarding progress, challenges, and potential solutions.

  • Maintain high standards in regulatory compliance, quality, and customer service.

  • Perform additional duties and projects as assigned.

Required Qualifications and Experience

  • Bachelor’s degree in Chemistry or a related scientific discipline.

  • Minimum 6 months of laboratory or industry experience in a relevant scientific environment.

  • Knowledge of Empower CDS and LIMS preferred, but not required.

  • Familiarity with GLP, cGMP, USP, and ICH guidelines preferred.

  • Strong verbal and written communication skills.

  • Ability to work independently and as part of a collaborative team.

  • Ability to lift up to 50 pounds, as required.

  • Must not be color-blind.

  • Occasional weekend work may be required.

Compensation

Estimated base salary range: USD 64,000 – 88,000 annually.
Actual compensation may vary based on experience, skills, location, and market conditions. This role may also qualify for discretionary bonuses, commissions, or long-term incentives.

Work Authorization

Candidates must be authorized to work in the United States. Visa sponsorship is not available for this role.

Benefits

Eligible employees may receive comprehensive benefits, including:

  • Medical and dental coverage beginning on day one

  • Life, accident, disability, and travel insurance

  • Employee Stock Purchase Plan (ESPP)

  • 401(k) Retirement Savings Plan with company match

  • Flexible Spending Accounts

  • Paid time off, holidays, family and medical leave, and parental leave

  • Employee Assistance Program (EAP)

  • Education assistance and professional development programs

  • Childcare benefits and commuting support

Equal Employment Opportunity

Baxter is an equal opportunity employer and evaluates applicants without regard to legally protected characteristics.

Reasonable Accommodations

Applicants requiring adjustments during the hiring process due to disability may request reasonable accommodations by contacting the recruitment team.

Recruitment Fraud Notice

Baxter advises applicants to be aware of fraudulent recruitment activities. Only engage with official Baxter recruiters and review Baxter’s Recruitment Fraud Notice for guidance.

Work Location

25212 W Illinois Route 120 RL/Drug
Round Lake, IL 60073
United States