Quality Manager

Baxter

Round Lake, Illinois, United States
Base: $112,000 - $154,000 annually; bonus: eligibl...
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5 years pharmaceutical quality experience
Cgmp fda eu pic/s regulatory knowledge
Cephalosporin segregation and contamination control
** Baxter is seeking a Quality Manager for its Round Lake, Illinois location, responsible for overseeing quality assurance in cephalosporin manufacturing operations. The ideal candidate will have at least five years of relevant experience, including supervisory roles, and strong knowledge of regulatory compliance in a pharmaceutical environment. **

Job Summary

  • The Quality Manager serves as the accountable quality leader ensuring compliant execution of manufacturing activities at the Round Lake Drug Delivery site.
  • Baxter's mission is to save and sustain lives, prioritizing quality over quantity in all decision-making processes.
  • The role offers comprehensive benefits including medical coverage starting day one, a 401(k) with company matching, and up to 35 days of paid time off.

Matching Summary

Match Score: 75

** Baxter is seeking a Quality Manager for its Round Lake, Illinois location, responsible for overseeing quality assurance in cephalosporin manufacturing operations. The ideal candidate will have at least five years of relevant experience, including supervisory roles, and strong knowledge of regulatory compliance in a pharmaceutical environment. **

Salary

Base: $112,000 - $154,000 annually; Bonus: Eligible for discretionary bonuses; Benefits: Comprehensive health, dental, 401(k), and PTO included

Skills & Requirements

Must-have

  • 5 years pharmaceutical quality experience
  • cGMP FDA EU PIC/S regulatory knowledge
  • Cephalosporin segregation and contamination control
  • Batch record review and CAPA execution
  • Direct QA oversight of manufacturing shifts

Nice-to-have

  • Experience with sterile injectable operations
  • Strong analytical problem-solving skills
  • Cross-functional collaboration capabilities
  • Leadership coaching and team development
  • Continuous improvement initiative drive

Key Requirements

  • Bachelor's degree in Science or Engineering
  • Minimum 5 years in pharmaceutical quality field
  • 1-2 years people leadership experience
  • US work authorization required (no sponsorship)

Work Rights

Must be authorized to work in the U.S.

Tailored Resume

Cover Letter