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Quality Team Leader

Job in Neenah, Winnebago County, Wisconsin, 54956, USA
Listing for: Kimberly-Clark
Full Time position
Listed on 2026-07-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Quality Engineering, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 105740 - 130620 USD Yearly USD 105740.00 130620.00 YEAR
Job Description & How to Apply Below

Job Description

Join the team behind iconic brands like Huggies®, Kleenex®, Cottonelle®, Scott®, Kotex®, Poise®, Depend®, and Kimberly-Clark Professional. At Kimberly-Clark, it’s all here for you—innovation, growth, and the chance to make a real impact.

In this role, you’ll help build and manage our portfolio of iconic, ground‑breaking brands, delivering better care for billions of people worldwide. It starts with you.

About You

In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.

Job Responsibilities
  • Provide leadership and coordination for the Neenah Cold Spring Facility quality management system by ensuring ongoing compliance to corporate/sector quality requirements.
  • Lead ongoing activities necessary to support existing products, including quality processes such as internal audits, management reviews, complaint handling, and corrective/preventive actions (CAPA).
  • Investigate and resolve product nonconformances and customer concerns, ensuring effective root cause analysis and corrective actions.
  • Partner with operations to provide data‑driven insights on product quality and process performance while promoting a strong safety and inclusive team culture.
  • Lead and develop the Quality Assurance team to support manufacturing operations and drive continuous quality improvement.
  • Maintain and strengthen the site’s Quality Management System to ensure compliance with corporate, sector, and regulatory requirements.
Required Qualifications
  • High School Diploma or higher.
  • 5+ years of experience in supervision, quality, or engineering.
  • Knowledge of or willingness to learn Enterprise systems such as SAP, Electron quality systems such as EtQ, current Good Manufacturing Practices with emphasis on FDA 21

    CFR Part 820, ISO 13485, CAPA, non‑conformance, Quality Test Data Systems (PASS), and LEAN manufacturing tools.
  • Track record of building working relationships and collaborative environments with functional areas within a manufacturing environment.
  • Ability to travel an appropriate amount of time to participate in efforts with staff and other manufacturing sites (
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