Quality Tech, Line Operations

0.6-1 years

$40,000 – $60,000

United States

10 Oct. 30, 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

Position Title: Quality Technician, Line Operations

Req ID: JR-189870
Location: Round Lake, Illinois, United States
Job Category: Quality / Manufacturing Support
Shift: Monday – Friday, 11:00 PM – 7:30 AM
Date Posted: —

🧭 Overview:

At Baxter, quality is the foundation of our mission to save and sustain lives.
As part of the Quality team, you play a crucial role in ensuring patient safety by maintaining the highest product standards throughout the lifecycle — from production to delivery.

Working in Quality at Baxter means continuous learning, collaboration with multiple departments, and opportunities to make a daily impact on people’s lives.

💡 Summary:

The Quality Technician (Line Operations) is responsible for performing activities that support Baxter’s quality systems.
This includes label control, sample management, documentation review, floor oversight, and in-process product inspections to ensure compliance with GMP and quality standards.

⚠️ Note: Candidate must not be allergic to penicillin or cephalosporin drugs.

🧩 Key Responsibilities:

Perform in-process product inspections and routine quality checks in finishing areas.
Provide floor shop oversight to ensure product and process compliance.
Conduct process compliance audits of manufacturing operations (TIQs).
Maintain department equipment and monitor inventory levels for controlled materials.
Manage monthly inventory cycle counts and follow up on variances.
Interact with manufacturing and supervision teams to address batch or quality issues.
Analyze data, record observations, and interpret results accurately.
Perform troubleshooting and make independent decisions based on procedural guidelines.
Support equipment validation testing through functional testing activities.
Identify and communicate process improvements to line supervision or management.
Support both Drug Delivery and Penicillin facilities as required.
Participate in continuous improvement initiatives to enhance product quality and process efficiency.

🧠 Qualifications & Skills Required:

Education:

High School Diploma or equivalent required.
Further education in science or technical fields preferred.

Experience:

Minimum 6 months of experience in manufacturing or quality (preferred).
Experience with cGMP and Good Documentation Practices (GDP) in pharma or medical device environments desirable.

Technical & Professional Skills:

Strong science, math, and computer skills (Microsoft Word, Excel).
Excellent written and verbal communication abilities.
Strong problem-solving and organizational skills.
Ability to work independently and within a team in a fast-paced, regulated environment.
Flexibility to work weekends and overtime when required.
Attention to detail and commitment to compliance and safety standards.

💰 Compensation:

Salary Range: $40,000 – $60,000 (USD) annually.
Actual pay may vary based on skills, experience, and location.

🌟 Benefits (U.S., except Puerto Rico):

Medical, Dental, and Vision coverage from Day One.
Life, Accident, and Disability Insurance (short- and long-term).
401(k) Retirement Savings Plan with company matching.
Employee Stock Purchase Plan (ESPP) – buy company stock at a discount.
Flexible Spending Accounts (FSA).
Educational Assistance Programs and Professional Development opportunities.
Paid Time Off (PTO): 20–35 days (based on tenure) + holidays.
Paid Parental Leave and Family/Medical Leave.
Employee Assistance Program (EAP) and Discount Programs.
Commuting and Childcare Benefits.

⚖️ Equal Employment Opportunity:

Baxter is an Equal Opportunity Employer.
All qualified applicants are considered without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, veteran status, or disability.

♿ Reasonable Accommodation:

Baxter provides reasonable accommodations to applicants with disabilities during the application and interview process.
If you require assistance, please contact Baxter through the official accommodation request link.

⚠️ Recruitment Fraud Notice:

Be aware of recruitment scams falsely claiming to represent Baxter.
Baxter does not request payment or sensitive financial details during recruitment.
Refer to Baxter’s Recruitment Fraud Notice for protection guidelines.

📍 Work Location:

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

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