Lead Quality Analyst

Kimberly-Clark

Beech Island, SC, United States
Base: 87,260 – 107,780 usd; bonus/equity: eligibil...
Own site quality management systems
Lead capa and quality nonconformance processes
Ensure compliance with gmp, iso, fda
You will own site Quality Management Systems, including ETQ modules, Approved Supplier Process, Equipment Calibration, and Document Control

Job Summary

  • You will own site Quality Management Systems, including ETQ modules, Approved Supplier Process, Equipment Calibration, and Document Control.
  • You will lead CAPA and Quality Nonconformance processes, including initiation, investigation, follow‑up, and closure for assigned systems.
  • You will develop, execute, and sustain continuous improvement initiatives for existing and new quality processes.

Matching Summary

You will own site Quality Management Systems, including ETQ modules, Approved Supplier Process, Equipment Calibration, and Document Control.

Salary

Base: 87,260 – 107,780 USD; Bonus/Equity: eligibility for a target bonus; Benefits: comprehensive benefits suite, 401(k) and Profit Sharing plan

Skills & Requirements

Must-have

  • Own site Quality Management Systems
  • Lead CAPA and Quality Nonconformance processes
  • Ensure compliance with GMP, ISO, FDA
  • Develop and maintain quality records systems
  • Partner with stakeholders for quality solutions

Nice-to-have

  • Problem-solver and connector
  • Thrives on creating order from complexity
  • Aligns with highest values of integrity
  • Winning with consumers and the market
  • Build and sustain organizational capability

Key Requirements

  • Bachelor’s degree in science, engineering or related discipline
  • 3+ years of broad experience in Quality, Manufacturing, Research or Regulatory function
  • Experience with FDA, Health Canada requirements for cosmetics and medical devices
  • Demonstrated LEAN/ Continuous Improvement skills
  • Demonstrated skill as a trainer

Work Rights

Not specified

Tailored Resume

Cover Letter