Quality Technician – Line Operations (Day Shift)
Job Category: Quality Assurance / Manufacturing / GMP Compliance
Reference ID: JR-194921
Location: Round Lake, Illinois, United States
Company: Baxter International Inc.
Shift: 2/2/3 Day Shift, 12-hour shifts (6:00 AM – 6:30 PM)
Employment Type: Full-Time
Work Authorization: U.S. work authorization required (no visa sponsorship available)
About the Organization
Baxter International Inc. is a global healthcare manufacturer dedicated to providing safe, high-quality therapies to patients worldwide. The company focuses on stringent quality assurance, compliance with GMP standards, and operational excellence across manufacturing sites, ensuring patient safety and regulatory adherence.
Position Overview
The Quality Technician – Line Operations (Day Shift) plays a critical role in ensuring product quality, compliance, and operational efficiency in Baxter’s manufacturing environment. This role involves floor oversight, quality checks, documentation, and supporting GMP-compliant operations for life-saving therapies. The position is ideal for candidates who are detail-oriented, collaborative, and comfortable working in a fast-paced, regulated manufacturing environment.
Key Responsibilities
Conduct floor shop oversight, routine inspections, and in-process product checks in finishing areas.
Perform quality compliance audits across manufacturing areas to ensure adherence to batch, process, and procedural standards (TIQs).
Collect, analyze, and interpret production data to identify trends or issues.
Maintain department equipment and controlled material inventory; perform monthly cycle counts and variance follow-up.
Perform troubleshooting, functional testing, and process compliance assessments.
Interact with manufacturing and supervision teams to resolve quality or batch-related concerns.
Identify process improvement opportunities and escalate to Line Operations supervision or management.
Adhere to GMP and documentation practices in a cleanroom environment.
Work independently and collaboratively to achieve quality and production goals.
Provide guidance or training to team members when required.
Ensure compliance with safety, procedural, and regulatory requirements in daily operations.
Required Qualifications & Experience
High School Diploma or equivalent; basic science, math, and computer literacy required.
Minimum 6 months of experience in manufacturing or quality assurance preferred.
Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices in pharmaceutical manufacturing preferred.
Strong communication, problem-solving, and team collaboration skills.
Ability to work in a fast-paced, dynamic environment with minimal supervision.
Must be able to work flexible hours, including every other weekend and overtime as needed.
Must not have allergies to penicillin or cephalosporin drugs.
Visual acuity of 20/20 near vision (corrective lenses allowed).
Shift & Work Environment
2/2/3 day shift schedule, 12-hour shifts from 6:00 AM to 6:30 PM.
Work will be performed in both Drug Delivery and Penicillin manufacturing facilities as needed.
Cleanroom environment with required garbing and strict adherence to sterile procedures.
Compensation & Benefits
Estimated base salary: $40,000 – $55,000 annually (based on location, experience, and skills).
Eligibility for overtime and discretionary bonuses.
Medical, dental, and vision coverage starting day one.
401(k) Retirement Savings Plan with company match.
Employee Stock Purchase Program (ESPP).
Paid holidays and 160 hours of PTO.
Paid parental leave, tuition reimbursement, and professional development opportunities.
Additional benefits: 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 are considered without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity, veteran status, disability, or any other legally protected characteristic.
Why Apply via ThePharmaDaily.com?
This role is ideal for candidates seeking career growth in pharmaceutical quality assurance, manufacturing operations, and GMP compliance. Join Baxter to gain hands-on experience in life-saving therapies, develop regulatory expertise, and contribute to a globally recognized healthcare organization.
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