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Quality Tech, Line Operations - 3rd Shift

Req # JR - 147060 Location Round Lake, Illinois, United States Job Category Quality Date posted 09/10/2024
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Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

  • Support for Parents

  • Continuing Education/ Professional Development

  • Employee Heath & Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential

Quality Tech, Line Operations - 3rd Shift

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This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. 

Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. 

Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. 

Your Role at Baxter

**This role is supporting 3rd shift: 11pm-7am**

The Quality Technician is responsible for performing a wide variety of assignments in label copy control, sample management, documentation review, and other quality department functions. This is a supporting role specifically for the manufacturing lines.

What you'll be doing

  • Makes detailed observations, analyze data, and interpret results.
  • Maintains department equipment and inventory levels for controlled materials.
  • Interacts with manufacturing and supervision on a daily basis to address quality process or batch related concerns.
  • Performs process compliance audits of all manufacturing areas to ensure quality of product/process is achieved.
  • Performs troubleshooting, works independently, and makes decisions based on general guidance and existing procedural requirements. 
  • Performs in process and/or final review of batch and/or critical systems documentation and determines acceptability by using standard operating procedures.  Ensures presence and acceptability of all required documentation prior to the release of the product and/or system.
  • Responsible for batch and/or critical systems review.  Achieves and maintains batch or systems release qualification within assigned production cell.
  • Reviews documentation such as protocols, CWRs, qualifications, etc. as assigned. 
  • Enters data into the Batch Release System.  Generates reports from Trackwise 8.
  • Performs product functional testing in support of equipment validations.

What you'll bring

  • Associate degree in related discipline or 6 months or more years related experience. 
  • Basic science, math, and computer skills (including Microsoft Word and Excel) are required.  
  • Good writing and verbal communication skills, and problem-solving skills are required.  
  • Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements 
  • It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities.
  • The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.
  • The ability to work some Saturdays is required.
  • Will work in both Drug Delivery and Penicillin facilities as needed. 
  • Overtime may be required to meet the production schedule.
  • *** The candidate must not be allergic to penicillin or cephalosporin drugs ***

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $40,000-$55,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law 
EEO is the law - Poster Supplement
Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

147060
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Address

Explore this location 25212 W Illinois Route 120 RL/Drug
Round Lake, IL 60073
United States of America
Explore This Location

Hear from Our Employees

Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

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