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 Ii (6pm-6:30am)

Baxter
Baxter
2+ years
$64,000 – $88,000 annually
Round Lake, United States
10 Feb. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 II – Night Shift
Job Category: Quality Assurance / Laboratory / Pharmaceutical Testing
Reference ID: JR-191304
Location: Round Lake, Illinois, United States
Company: Baxter International Inc.
Shift: Night Shift 6:00 PM – 6:30 AM, Rotating 2-2-3 Schedule (Weekends Included)
Employment Type: Full-Time
Work Authorization: U.S. work authorization required (no visa sponsorship available)


About the Organization

Baxter International Inc. is a global leader in healthcare solutions, committed to producing high-quality biologics and pharmaceutical products. The company prioritizes patient safety, regulatory compliance, and operational excellence, offering employees opportunities for professional growth in a collaborative, innovation-driven environment.


Position Overview

The Quality Lab Associate II provides critical laboratory support for pharmaceutical product testing, environmental monitoring, and quality assurance programs. This night-shift role ensures compliance with Good Laboratory Practices (GLP), Current Good Manufacturing Practices (cGMP), and FDA regulatory standards while maintaining product integrity and patient safety.

This position is suitable for candidates with strong analytical skills, attention to detail, and the ability to work independently in a fast-paced, regulated laboratory environment.


Key Responsibilities

  • Conduct biological, chemical, and physical analyses on raw materials, in-process materials, and finished pharmaceutical products.

  • Perform environmental monitoring testing and assessments within the manufacturing facility.

  • Utilize laboratory instrumentation, including HPLC, GC, and LIMS, to collect, record, and analyze data.

  • Review and document test results in compliance with SOPs, regulatory guidelines, and company quality standards.

  • Investigate deviations and prepare OOL/OOS/OOT documentation.

  • Mentor and provide training to Quality Laboratory Associate I (QLA I) team members.

  • Participate in laboratory and manufacturing audits, update SOPs, and maintain equipment calibration and maintenance.

  • Support improvement initiatives using LEAN management principles, including 6S and Kaizen methodologies.

  • Collaborate with peers and management to address process challenges, improve efficiency, and ensure regulatory compliance.

  • Maintain a clean, organized, and safe laboratory environment and ensure adherence to safety protocols.


Required Qualifications & Experience

  • Bachelor’s degree in Chemistry, Biochemistry, or Physical Science.

  • Minimum 2 years of laboratory or pharmaceutical quality experience required.

  • Strong oral and written communication skills; highly analytical and detail-oriented.

  • Advanced laboratory skills with understanding of statistical methods and analytical principles.

  • Knowledge of cGMP, GLP, USP, ICH guidelines preferred.

  • Experience with laboratory information systems (LIMS) and Empower Chromatography Data System is a plus.

  • Ability to mentor junior laboratory staff and provide technical guidance.

  • Rotating weekend availability and ability to lift up to 50 pounds.

  • Visual acuity 20/25 near vision with or without corrective lenses; must not be color blind.

  • Candidate must not be allergic to Penicillin, Cephalosporin, or related materials.


Shift & Work Environment

  • Night Shift: 6:00 PM – 6:30 AM, rotating 2-2-3 schedule including weekends.

  • Work in a cleanroom and controlled laboratory environment.

  • Dynamic, regulated pharmaceutical manufacturing setting requiring adherence to SOPs and safety protocols.


Compensation & Benefits

  • Estimated base salary: $64,000 – $88,000 annually, depending on skills, experience, and location.

  • Eligibility for discretionary bonuses and long-term incentives.

  • Medical, dental, and vision coverage effective from day one.

  • 401(k) Retirement Savings Plan with company match.

  • Employee Stock Purchase Program (ESPP).

  • Paid holidays, PTO, parental leave, and tuition reimbursement.

  • Employee Assistance Program (EAP), commuting benefits, childcare support, and employee discounts.


Equal Employment Opportunity

Baxter International Inc. is an Equal Opportunity Employer. All qualified applicants will be considered without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, veteran status, disability, or other legally protected characteristics.