Quality Manager - Beech Island

Kimberly-Clark

Beech Island, SC, United States
Base: 127,600 – 157,600 usd; bonus/equity: target ...
Not specified (assumed onsite)
Quality management system (qms) compliance
Fda class 1 medical device regulations
Finished product specification (fps) adherence
Kimberly-Clark is seeking a Quality Manager for its Beech Island facility, responsible for establishing and maintaining a robust Quality Management System compliant with various FDA regulations. The ideal candidate will have extensive experience in quality roles within a manufacturing environment, demonstrating leadership and a commitment to quality

Job Summary

  • The Plant Quality Manager is responsible for establishing and maintaining a robust Quality Management System compliant with FDA Medical Device, FDA Cosmetics, and Consumer Product requirements.
  • Kimberly-Clark offers a comprehensive benefits package including medical, dental, vision coverage, flexible spending accounts, and support for education and family needs.
  • The role drives a culture of quality across the manufacturing facility aligned with strategic quality plans and business objectives.

Matching Summary

Match Score: 85

Kimberly-Clark is seeking a Quality Manager for its Beech Island facility, responsible for establishing and maintaining a robust Quality Management System compliant with various FDA regulations. The ideal candidate will have extensive experience in quality roles within a manufacturing environment, demonstrating leadership and a commitment to quality.

Salary

Base: 127,600 – 157,600 USD; Bonus/Equity: Target bonus eligibility; Benefits: Comprehensive benefits including 401(k) and Profit Sharing

Skills & Requirements

Must-have

  • Quality Management System (QMS) compliance
  • FDA Class 1 Medical Device regulations
  • Finished Product Specification (FPS) adherence
  • CAPA and QNC management
  • Internal audit planning and execution
  • Supplier quality management and SCAR process
  • Calibration of test equipment

Nice-to-have

  • Mentorship and coaching of quality professionals
  • Driving quality culture and strategic quality planning
  • Cross-functional stakeholder engagement
  • Alignment with company core values and ways of working
  • Experience with 3rd party and regulatory audits

Key Requirements

  • Bachelor’s degree in scientific or engineering discipline
  • 7+ years manufacturing quality experience
  • People leadership and succession planning
  • Experience with FDA Medical Device and Cosmetics regulations
  • Quality Management Representative experience in audits

Work Rights

Not specified

Tailored Resume

Cover Letter