Quality Lab Associate II – 1st Shift (Monday–Friday)
Location: Round Lake, Illinois, United States
Job ID: JR-192169
Company: Baxter International
About the Role
Baxter is dedicated to improving patient safety and advancing global healthcare. As a Quality Lab Associate II, you will support the full product lifecycle by performing biological, chemical, and physical analyses on pharmaceutical products, including biologics, drug products, raw materials, and environmental monitoring samples. This role directly contributes to Baxter’s mission to save and sustain lives.
This is a 1st shift, full-time position (Monday–Friday).
Note: Candidates must not be allergic to Penicillin, Cephalosporin, or related materials.
Key Responsibilities
Laboratory Testing & Data Review
Perform chemical and physical analysis on raw materials, in-process samples, finished products, and environmental monitoring samples.
Conduct advanced assays using instruments such as HPLC and GC.
Record and review data in LIMS and other computerized systems.
Maintain documentation in compliance with FDA, GLP, QSR, and cGMP requirements.
Complete project-based or protocol-driven testing within required timelines.
Quality & Compliance
Ensure data integrity and accurate quality records in notebooks and controlled documents.
Audit laboratory and manufacturing processes; update SOPs when required.
Investigate deviations and prepare OOS/OOT/OOL documents.
Support continuous improvement initiatives using Lean principles (6S, Kaizen).
Team Support & Training
Work under minimal supervision.
Mentor and provide training to Quality Lab Associate I team members.
Communicate proactively with management and peers to report progress and resolve issues.
Operational Excellence
Perform equipment maintenance and calibrations.
Maintain a clean, safe, and compliant laboratory environment.
Participate in cross-functional initiatives to enhance efficiency and product quality.
Required Qualifications
Education
Bachelor’s degree in Chemistry or a related physical science.
Experience
Minimum 2+ years of laboratory or pharmaceutical industry experience.
Experience with cGMP/GLP environments preferred.
Familiarity with Empower Chromatography Data System and LIMS is an advantage.
Technical Skills
Strong analytical and advanced laboratory skills.
Knowledge of USP, ICH guidelines, and regulatory expectations.
Ability to manage multiple tasks independently under deadlines.
Strong documentation, communication, and problem-solving abilities.
Additional Requirements
Ability to lift up to 50 lbs when necessary.
Must not be color blind.
Occasional weekend work may be required.
Ability to work both independently and collaboratively in a dynamic environment.
Compensation
Estimated base salary range: USD 64,000 – 88,000 annually
Actual compensation may vary based on skills, experience, and location. Candidates may also be eligible for bonuses, incentives, and additional benefits.
Benefits
Baxter offers a comprehensive benefits package for eligible employees, including:
Medical, dental, and life insurance (coverage from day one)
Disability insurance and business travel insurance
401(k) Retirement Savings Plan with company match
Employee Stock Purchase Plan (ESPP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays and paid time off (20–35 days based on tenure)
Parental leave and family medical leave
Commuter benefits, employee discount programs, and childcare benefits
Work Authorization
Applicants must be legally authorized to work in the United States.
Visa sponsorship is not available for this role.
Equal Employment Opportunity
Baxter is an equal opportunity employer and evaluates applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, veteran status, or disability.
Location
25212 W Illinois Route 120
Round Lake, IL 60073
United States
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