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Quality Technician

https://www.baxter.com/ Logo

Baxter

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Location:
United States , Round Lake

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Contract Type:
Employment contract

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Salary:

40000.00 - 55000.00 USD / Year

Job Description:

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.

Job Responsibility:

  • Makes detailed observations, analyzes data, and interprets results
  • Maintains department equipment and inventory levels for controlled materials
  • Owns monthly inventory cycle count initiation and variance follow-up
  • Perform routine inspections as the provider of floor shop oversight, quality checks, and in-process product inspections of finishing product areas
  • Interacts with manufacturing and supervision to address quality process or batch-related concerns
  • Performs process compliance audits of all manufacturing areas to ensure quality of product/process (TIQs) is achieved
  • Performs troubleshooting, works independently, and makes decisions based on general guidance and existing procedural requirements
  • Performs product functional testing in support of equipment validations
  • Identifies process improvements and escalates to Line Operations Supervision and/or Management
  • Ability to work independently and as part of a team in a fast-paced environment

Requirements:

  • Candidate must not be allergic to penicillin or cephalosporin drugs
  • 6 months of experience in manufacturing/quality preferred
  • HS Diploma or equivalent is required
  • Basic science, math, and computer skills (including Microsoft Word and Excel) are required
  • Good writing, verbal communication, 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
  • Candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision
  • Will work in both Drug Delivery and Penicillin facilities as needed
  • Overtime may be required to meet the production schedule
  • Must be able to work every other weekend
  • Visual Acuity 20/20 Near Vision with or without corrective vision required
  • Applicants must be authorized to work for any employer in the U.S.
What we offer:
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP) with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP) with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • Childcare benefits

Additional Information:

Job Posted:
May 03, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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