Lead Quality Analyst

KC IABC

Beech Island, SC, United States
Base: 87,260 – 107,780 usd; bonus/equity: eligibil...
Not specified (assumed on-site).
Quality management systems ownership
Capa and nonconformance process leadership
Audit readiness and qa training support
The Lead Quality Analyst position at Kimberly-Clark involves managing quality systems and processes to ensure compliance with regulatory standards while driving continuous improvement initiatives. The ideal candidate will have a background in quality assurance, strong analytical skills, and experience in a manufacturing or regulatory environment

Job Summary

  • You will help deliver better care for billions of people around the world by leading quality systems and continuous improvement efforts.
  • This role offers a comprehensive benefits suite including 401(k), Profit Sharing plan, and eligibility for a target bonus.
  • Kimberly-Clark is committed to diversity, inclusion, and equal opportunity employment while supporting relocation for the chosen candidate.

Matching Summary

Match Score: 85

The Lead Quality Analyst position at Kimberly-Clark involves managing quality systems and processes to ensure compliance with regulatory standards while driving continuous improvement initiatives. The ideal candidate will have a background in quality assurance, strong analytical skills, and experience in a manufacturing or regulatory environment.

Salary

Base: 87,260 – 107,780 USD; Bonus/Equity: Eligibility for target bonus; Benefits: Comprehensive benefits including 401(k) and Profit Sharing plan

Skills & Requirements

Must-have

  • Quality Management Systems ownership
  • CAPA and Nonconformance process leadership
  • Audit readiness and QA training support
  • Compliance with GMP, ISO, FDA regulations
  • Continuous improvement execution
  • Quality systems technical expertise
  • Statistical process control and inspection

Nice-to-have

  • LEAN/Continuous Improvement skills
  • Strong analytical and trend analysis skills
  • Prior leadership experience on projects
  • Collaborative and integrity-driven mindset
  • Supplier and cross-functional partnership

Key Requirements

  • Bachelor’s degree in science or engineering
  • 3+ years experience in Quality or Regulatory functions
  • Knowledge of FDA, Health Canada regulations
  • Experience with formulated cosmetics and medical devices
  • LEAN/Continuous Improvement application
  • Six Sigma Black or Green Belt preferred
  • ASQ Quality Engineer or Auditor certifications preferred
  • ISO 9001 or 13485 Lead Auditor certification preferred

Work Rights

Not specified

Tailored Resume

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